Sunday, 8 July 2012

Alphanate


Generic Name: antihemophilic factor viii and von willebrand factor complex (Intravenous route)


an-tee-hee-moe-FIL-ik FAK-tor ATE HUE-man, Von WILL-a-brand FAK-tor KOM-plex (HUE-man)


Commonly used brand name(s)

In the U.S.


  • Alphanate

  • Humate-P

  • Wilate

Available Dosage Forms:


  • Powder for Solution

Therapeutic Class: Antihemophilic Agent


Uses For Alphanate


Antihemophilic Factor VIII and von Willebrand Factor Complex injection is a combination product that is used to treat serious bleeding episodes in patients with a bleeding problem called von Willebrand disease (VWD). The bleeding episode may be related to an injury (trauma) or a surgical procedure. This medicine may also be used to stop bleeding in patients with hemophilia A.


Antihemophilic Factor VIII and von Willebrand Factor Complex are normally produced in the body. They help clot the blood when an injury occurs. Patients with von Willebrand disease or hemophilia A do not make enough of these substances to prevent bleeding, so this product is given to increase the levels of these substances in the blood.


This medicine is available only with your doctor's prescription. This medicine is to be administered only by or under the supervision of your doctor.


Before Using Alphanate


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of Antihemophilic Factor VIII and von Willebrand Factor Complex injection in children 5 to 16 years of age.


Geriatric


Adequate and well-controlled studies have not been done on the relationship of age to the effects of Antihemophilic Factor VIII and von Willebrand Factor Complex injection in geriatric patients.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


Studies in women suggest that this medication poses minimal risk to the infant when used during breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Blood clots or a history of medical problems caused by blood clots—Use with caution. These conditions may increase the risk of developing blood clots.

Proper Use of antihemophilic factor viii and von willebrand factor complex

This section provides information on the proper use of a number of products that contain antihemophilic factor viii and von willebrand factor complex. It may not be specific to Alphanate. Please read with care.


A nurse or other trained health professional will give you this medicine. This medicine is given through a needle placed in one of your veins.


Precautions While Using Alphanate


It is very important that your doctor check you or your child closely while you are receiving this medicine to make sure it is working properly. Blood tests may be needed to check for unwanted effects.


This medicine may cause a serious type of allergic reaction called anaphylaxis. Anaphylaxis can be life-threatening and requires immediate medical attention. Tell your doctor or nurse right away if you or your child have a cough; difficulty with swallowing; dizziness; a fast heartbeat; wheezing; shortness of breath; trouble with breathing; chest tightness; swelling in your face, hands, tongue, or throat; a fever; chills; a runny nose or sneezing; itching or hives; or lightheadedness or faintness after you get the injection.


This medicine may increase your chance of having blood clotting problems. Tell your doctor right away if you or your child have a sudden or severe headache, problems with vision or speech, chest pain, shortness of breath, or numbness or weakness while you are receiving this medicine.


This medicine is made from donated human blood. Some human blood products have transmitted certain viruses to people who have received them. The risk of getting a virus from medicines made from human blood has been greatly reduced in recent years. This is the result of required testing of human donors for certain viruses, and testing during the making of these medicines. Although the risk is low, talk with your doctor if you have concerns.


Alphanate Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


More common
  • Difficulty with breathing or swallowing

  • dizziness

  • fast heartbeat

  • fever

  • hives or welts

  • itching

  • nausea

  • reddening of the skin, especially around the ears

  • shortness of breath

  • skin rash

  • swelling of the face, throat, or tongue

  • unusual tiredness or weakness

Incidence not known
  • Cough

  • tightness in the chest

  • vomiting

  • wheezing

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Alphanate side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Alphanate resources


  • Alphanate Side Effects (in more detail)
  • Alphanate Use in Pregnancy & Breastfeeding
  • Alphanate Support Group
  • 0 Reviews for Alphanate - Add your own review/rating


  • Alphanate Prescribing Information (FDA)

  • Alphanate MedFacts Consumer Leaflet (Wolters Kluwer)

  • Humate-P Prescribing Information (FDA)

  • Humate-P MedFacts Consumer Leaflet (Wolters Kluwer)

  • Wilate Consumer Overview

  • Wilate MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Alphanate with other medications


  • Hemophilia A
  • von Willebrand's Disease

Bisodol Extra Strong Mint Tablets





1. Name Of The Medicinal Product



Bisodol Extra Strong Mint Tablets


2. Qualitative And Quantitative Composition



Active ingredients per tablet:










Calcium Carbonate Ph.Eur.




522mg




Magnesium Carbonate Light Ph.Eur.




68mg




Sodium Bicarbonate Ph.Eur.




64mg



3. Pharmaceutical Form



Chewable tablet.



4. Clinical Particulars



4.1 Therapeutic Indications



For relief from indigestion, dyspepsia, heartburn, acidity and flatulence.



4.2 Posology And Method Of Administration



Adults, elderly and children over 12 years:



Take one or two tablets as required. Suck slowly or chew as preferred.



Children below 12 years:



Not recommended.



4.3 Contraindications



Hypophosphataemia, and avoid in patients with heart or renal failure.



4.4 Special Warnings And Precautions For Use



The label will contain the following statements:



1. If symptoms persist, consult your doctor.



2. Keep all medicines out of the reach of children.



3. Not to be taken during the first three months of pregnancy.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Antacids are known to reduce the absorption of certain medicines including tetracyclines and iron salts.



4.6 Pregnancy And Lactation



No clinical data on exposed pregnancies are available.



Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development (see section 5.3).



Caution should be exercised when prescribing to pregnant women.



4.7 Effects On Ability To Drive And Use Machines



None stated.



4.8 Undesirable Effects



Calcium salts can have a constipating effect and magnesium salts can have a laxative effect. The mixture of antacids is intended to avoid the lower gastrointestinal effects seen with single antacid preparations. No side effects associated with sodium bicarbonate except when taken in excess. Rebound hyperacidity may occur with prolonged dosage.



4.9 Overdose



Hypermagnesaemia – intravenous administration of calcium salts.



Hypernatraemia – give plenty of salt free liquids.



Hypercalcaemia – remove source of calcium.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Sodium bicarbonate, calcium carbonate and magnesium carbonate are antacids. They act by neutralising the hydrochloric acid produced by the stomach and thus reducing gastric and duodenal irritation.



Sodium Bicarbonate



Sodium bicarbonate is a rapid onset, short acting antacid which neutralises acid secretions in the gastrointestinal tract by reacting with hydrochloric acid to produce sodium chloride. During neutralisation carbon dioxide is released, facilitating erucation which provides a sense of relief.



Calcium Carbonate



Calcium carbonate is an antacid with a more prolonged effect than sodium bicarbonate. It rapidly reacts with gastric acid to produce calcium chloride.



Magnesium Carbonate



Magnesium carbonate reacts with gastric acid to form soluble magnesium chloride and carbon dioxide. Because of its crystalline structure it reacts less rapidly than sodium bicarbonate giving it a slower onset of action, and providing longer lasting relief.



5.2 Pharmacokinetic Properties



Sodium Bicarbonate



Administration of sodium bicarbonate by mouth causes neutralisation of gastric acid with the production of carbon dioxide. Bicarbonate not involved in that reaction is absorbed and in the absence of a deficit of bicarbonate in the plasma, bicarbonate ions are excreted in the urine that is rendered alkaline with an accompanying diuresis.



Calcium Carbonate



Calcium carbonate is converted to calcium chloride by gastric acid. Some of the calcium is absorbed from the intestines but about 85% is reconverted to insoluble calcium salts, such as the carbonate and is excreted in the faeces.



Magnesium Carbonate



Magnesium carbonate reacts with gastric acid to form soluble magnesium chloride and carbon dioxide in the stomach. Some magnesium is absorbed but is usually excreted rapidly in the urine.



5.3 Preclinical Safety Data



The active ingredients in Bisodol Tablets have a well-established safety record.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Saccharin Soluble



Starch



Sucrose



Calcium Stearate



Peppermint Essential Oil



6.2 Incompatibilities



None known.



6.3 Shelf Life



60 months.



6.4 Special Precautions For Storage



Store at a temperature not exceeding 25°C.



6.5 Nature And Contents Of Container












Tablets in a polypropylene container with polypropylene lid.


 


Pack size:



30


Carton of 5 rolls of 20 tablets in wax laminated foil with paper label.


 


Pack size:




100



6.6 Special Precautions For Disposal And Other Handling



None.



7. Marketing Authorisation Holder



Forest Laboratories UK Limited



Riverbridge House



Anchor Boulevard



Crossways Business Park



Dartford



Kent DA2 6SL.



U.K.



8. Marketing Authorisation Number(S)



PL 0108/0125



9. Date Of First Authorisation/Renewal Of The Authorisation



22nd November 1993/26th May 2004



10. Date Of Revision Of The Text



March 2010



11. Legal Category


GSL




Friday, 6 July 2012

Boots Pharmacy Cold and Flu Night Capsules





Boots Pharmacy Cold & Flu Night Capsules



Please read all of this leaflet carefully because it contains important information for you.


This medicine is available without prescription to treat minor conditions. However, you still need to take it carefully to get the best results from it.


  • Keep this leaflet, you may need to read it again

  • Ask your pharmacist if you need more information or advice




What this medicine is for


This medicine contains paracetamol, an analgesic, which relieves pain and reduces fever, a decongestant to relieve a blocked up nose and a cough suppressant to relieve coughing. It also contains an antihistamine, which causes drowsiness and helps you to get a restful night's sleep.


It can be used to relieve even the worst symptoms of colds and flu during the night, and to help you get a restful night's sleep.




Before you take this medicine


This medicine can be taken by adults and children over the age of 12. However, some people should not take this medicine or should seek the advice of their pharmacist or doctor first.



Do not take:



  • If you are pregnant or breastfeeding


  • If you are allergic to any of the ingredients


  • If you have heart disease or have high blood pressure (including that due to a tumour near your kidneys)


  • If you suffer from hyperexcitability, diabetes, an overactive thyroid, enlarged prostate, or high pressure in the eye (glaucoma)


  • If you suffer from severe liver or kidney problems, chronic bronchitis or bronchiectasis


  • If you are taking monoamine oxidase inhibitors (for depression) or have taken them within the last 14 days



Talk to your pharmacist or doctor:


  • If you have asthma



Other important information



Driving and using machinery: This medicine may cause drowsiness or dizziness. You should not drive or operate machinery until you are sure you are not affected.



Do not drink alcohol (e.g. wine, beer, spirits) whilst taking this medicine.



Information about some of the ingredients in this medicine: The colour ponceau 4R (E124) may cause allergic reactions.




Taking other medicines



This medicine contains paracetamol. Do not take with any other paracetamol-containing products.


Before you take these capsules, make sure that you tell your pharmacist about ANY other medicines you might be using at the same time, particularly the following:


  • Barbiturates, sleeping tablets, strong painkillers, sedatives or tranquillisers (because the Night capsules may make you feel more sleepy for a longer time)

  • Tricyclic antidepressants and atropine like medicines such as antihistamines or other medicines which may cause a dry mouth (you may have more risk of having some of the side effects)

  • Medicines for high blood pressure (your blood pressure may increase whilst you are taking this medicine)

  • Digoxin for heart problems (this may make your heart beat too fast)

  • Domperidone or metoclopramide, for nausea and vomiting (may increase the effect of the painkiller in this medicine)

  • Colestyramine, for lowering blood lipid levels (may reduce the effect of the painkiller in this medicine)

  • Warfarin or other coumarins (for thinning the blood) - If you take warfarin you can take occasional doses of this medicine, but talk to your doctor first before you take it on a regular basis

If you are unsure about interactions with any other medicines, talk to your pharmacist. This includes medicines prescribed by your doctor or medicine you have bought for yourself including herbal and homeopathic remedies.





How to take this medicine


Check that the foil is not broken before use.


If it is discard the capsule.



  • Adults and children of 12 years and over


  • Take two capsules at bedtime only

Swallow each capsule whole with water.


Do not give to children under 12 years.


Do not take more than the dose recommended above.


Do not take this medicine for more than 7 days unless your doctor agrees.


If symptoms persist consult your doctor.



If you take too many capsules: Immediate medical advice should be sought in the event of an overdose, even if you feel well, because of the risk of delayed, serious liver damage. Go to your nearest hospital casualty department. Take your medicine and this leaflet with you.




Possible side effects


Most people will not have problems, but some may get some.



If you get any of these serious side effects, stop taking the capsules. See a doctor at once:


  • Difficulty in breathing, swelling of the face, neck, tongue or throat (severe allergic reactions)


These other effects are less serious. If they bother you talk to a pharmacist:


  • Drowsiness, tiredness, dizziness, muscular weakness

  • Feeling sick, being sick, diarrhoea, constipation, stomach pain

  • Headache, blurred vision, ringing in the ears, loss of appetite

  • Irritability, nightmares

  • Hallucinations, particularly in children

  • Difficulty in passing urine, dry mouth, fast heart rate, tremors, skin rashes

  • Unusual bruising, or infections such as sore throats - that may be a sign of very rare changes in the blood


If any side effect becomes severe, or if you notice any side effect not listed here, please tell your pharmacist or doctor.




How to store this medicine


Keep this medicine in a safe place out of the sight and reach of children, preferably in a locked cupboard.


Do not use this medicine after the "Use by" date on the carton.


Do not store above 25°C.


Store it in the original package.




What is in this medicine


Each capsule contains Diphenhydramine Hydrochloride 12.5 mg, Paracetamol 500 mg, Pholcodine 5 mg, Pseudoephedrine Hydrochloride 30 mg, which are the active ingredients.


As well as the active ingredients, the capsules also contain sodium lauryl sulphate, sodium starch glycolate, magnesium stearate. The capsule shell contains gelatin and colours, which are; brilliant blue (E133), black iron oxide (E172), titanium dioxide (E171), ponceau 4R (E124) and Opacode white (printing ink containing titanium dioxide (E171), shellac, soya lecithin, Antifoam DC 1510).


This pack contains 12 blue and purple capsules with 0581 and BOOTS printed in white.




Who makes this medicine


Manufactured for the Marketing Authorisation holder



Boots Pharmacy

Nottingham

NG2 3AA


by



Hamol Limited

Nottingham

NG90 2DB


PL00014/0581


Leaflet prepared October 2007


If you would like any further information about this product, please contact The Boots Company PLC Nottingham NG2 3AA.




Other formats


To request a copy of this leaflet in Braille, large print or audio please call, free of charge:


0800 198 5000 (UK only)


Please be ready to give the following information:


Product name: Boots Pharmacy Cold & Flu Night Capsules


Reference number: 00014/0581


This is a service provided by the Royal National Institute of the Blind.



BTC22867 vs D 16/01/08





Wednesday, 4 July 2012

linagliptin


Generic Name: linagliptin (LIN a GLIP tin)

Brand Names: Tradjenta


What is linagliptin?

Linagliptin is an oral diabetes medicine that helps control blood sugar levels. It works by regulating the levels of insulin your body produces after eating.


Linagliptin is used together with diet and exercise to treat type 2 diabetes. Linagliptin is not for treating type 1 diabetes.


Linagliptin may also be used for purposes not listed in this medication guide.


What is the most important information I should know about linagliptin?


Do not use this medication if you are allergic to linagliptin or if you are in a state of diabetic ketoacidosis (call your doctor for treatment with insulin).

Before you take linagliptin, tell your doctor if you have high cholesterol or triglycerides, or a history of pancreatitis.


Stop taking linagliptin and call your doctor at once if you have severe pain in your upper stomach spreading to your back, nausea and vomiting, loss of appetite, or fast heart rate.

Low blood sugar (hypoglycemia) can occur if you skip a meal, exercise too long, drink alcohol, or are under stress. Symptoms include headache, hunger, weakness, sweating, tremors, irritability, or trouble concentrating. Carry hard candy or glucose tablets with you in case you have low blood sugar. Other sugar sources include orange juice and milk. Be sure your family and close friends know how to help you in an emergency.


Linagliptin is only part of a complete program of treatment that may also include diet, exercise, weight control, foot care, eye care, dental care, and testing your blood sugar. Follow your diet, medication, and exercise routines very closely. Changing any of these factors can affect your blood sugar levels.


Your blood sugar will need to be checked often, and you may need other blood tests at your doctor's office. Visit your doctor regularly.


What should I discuss with my healthcare provider before taking linagliptin?


Do not use this medication if you are allergic to linagliptin, or if you are in a state of diabetic ketoacidosis (call your doctor for treatment with insulin).

To make sure you can safely take linagliptin, tell your doctor if you have any of these other conditions:



  • high cholesterol or triglycerides (a type of fat in the blood); or




  • a history of pancreatitis.




FDA pregnancy category B. Linagliptin is not expected to harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether linagliptin passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Do not give this medication to anyone under 18 years old without medical advice.

How should I take linagliptin?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Your doctor may occasionally change your dose to make sure you get the best results.


Linagliptin is usually taken once per day. You may take this medicine with or without food. Follow your doctor's instructions.


Your blood sugar will need to be checked often, and you may need other blood tests at your doctor's office. Visit your doctor regularly.


Know the signs of low blood sugar (hypoglycemia) and how to recognize them: headache, hunger, weakness, sweating, tremor, irritability, or trouble concentrating.

Always keep a source of sugar available in case you have symptoms of low blood sugar. Sugar sources include orange juice, glucose gel, candy, or milk. If you have severe hypoglycemia and cannot eat or drink, use an injection of glucagon. Your doctor can give you a prescription for a glucagon emergency injection kit and tell you how to give the injection.


Check your blood sugar carefully during a time of stress or illness, if you travel, exercise more than usual, drink alcohol, or skip meals. These things can affect your glucose levels and your dose needs may also change.


Your doctor may want you to stop taking linagliptin for a short time if you become ill, have a fever or infection, or if you have surgery or a medical emergency. Ask your doctor how to adjust your linagliptin dose if needed. Do not change your medication dose or schedule without your doctor's advice.

Linagliptin is only part of a complete program of treatment that may also include diet, exercise, weight control, foot care, eye care, dental care, and testing your blood sugar. Follow your diet, medication, and exercise routines very closely. Changing any of these factors can affect your blood sugar levels.


Store at room temperature away from moisture and heat.

See also: Linagliptin dosage (in more detail)

What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

You may have signs of low blood sugar, such as extreme weakness, blurred vision, sweating, trouble speaking, tremors, stomach pain, confusion, and seizure (convulsions).


What should I avoid while taking linagliptin?


Follow your doctor's instructions about any restrictions on food, beverages, or activity.


Linagliptin side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Stop taking linagliptin and call your doctor at once if you have a serious side effect such as:

  • pancreatitis - severe pain in your upper stomach spreading to your back, nausea and vomiting, loss of appetite, fast heart rate; or




  • fever, sore throat, and headache with a severe blistering, peeling, and red skin rash.



Less serious side effects may include:



  • runny or stuffy nose, sore throat;




  • cough;




  • weight gain;




  • muscle or joint pain;




  • headache; or




  • back pain.



This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


Linagliptin Dosing Information


Usual Adult Dose for Diabetes Mellitus Type II:

5 mg orally once daily.


What other drugs will affect linagliptin?


Tell your doctor about all other medicines you use, especially:



  • bosentan (Tracleer);




  • dexamethasone (Cortastat, Dexasone, Solurex, DexPak);




  • ketoconazole (Nizoral);




  • quinidine (Quin-G);




  • rifabutin (Mycobutin), rifampin (Rifadin, Rifater, Rifamate), or rifapentine (Priftin);




  • St. John's wort;




  • verapamil (Calan, Covera, Isoptin, Verelan);




  • a barbiturate such as butabarbital (Butisol), secobarbital (Seconal), pentobarbital (Nembutal), or phenobarbital (Solfoton);




  • HIV/AIDS medication such as efavirenz (Sustiva, Atripla), etravirine (Intelence), nelfinavir (Viracept), nevirapine (Viramune), ritonavir (Norvir, Kaletra), or saquinavir (Invirase);




  • medicines to treat narcolepsy, such as armodafanil (Nuvigil) or modafanil (Progivil);




  • medicines used to prevent organ transplant rejection, such as cyclosporine (Gengraf, Neoral, Sandimmune) or tacrolimus (Prograf); or




  • seizure medication such as carbamazepine (Carbatrol, Tegretol), felbamate (Felbatol), oxcarbazepine (Trileptal), phenytoin (Dilantin), or primidone (Mysoline).



Although linagliptin is not as likely to cause hypoglycemia (low blood sugar) as some other oral diabetes medications, tell your doctor if you are taking any other drugs that can potentially lower blood sugar, such as:



  • probenecid (Benemid);




  • nonsteroidal anti-inflammatory drugs (NSAIDs);




  • aspirin or other salicylates (including Pepto-Bismol);




  • sulfa drugs (Bactrim and others);




  • a monoamine oxidase inhibitor (MAOI);




  • another oral diabetes medication such as glipizide (Glucotrol, Metaglip), glimepiride (Amaryl, Avandaryl, Duetact), glyburide (DiaBeta, Micronase, Glucovance), and others.




  • beta-blockers (Tenormin and others); or



This list is not complete and other drugs may interact with linagliptin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More linagliptin resources


  • Linagliptin Side Effects (in more detail)
  • Linagliptin Dosage
  • Linagliptin Use in Pregnancy & Breastfeeding
  • Linagliptin Drug Interactions
  • Linagliptin Support Group
  • 5 Reviews for Linagliptin - Add your own review/rating


  • linagliptin Advanced Consumer (Micromedex) - Includes Dosage Information

  • Linagliptin Professional Patient Advice (Wolters Kluwer)

  • Linagliptin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Tradjenta Prescribing Information (FDA)

  • Tradjenta Consumer Overview



Compare linagliptin with other medications


  • Diabetes, Type 2


Where can I get more information?


  • Your pharmacist can provide more information about linagliptin.

See also: linagliptin side effects (in more detail)


Tuesday, 3 July 2012

Adderall



Generic Name: dextroamphetamine and amphetamine (Oral route)


am-FET-a-meen a-SPAR-tate, am-FET-a-meen SUL-fate, dex-troe-am-FET-a-meen SAK-a-rate, dex-troe-am-FET-a-meen SUL-fate


Oral route(Tablet;Capsule, Extended Release)

Amphetamines have a high potential for abuse, and administration for prolonged periods of time may lead to drug dependence and must be avoided. Misuse of amphetamines may cause sudden death and serious cardiovascular adverse events .



Commonly used brand name(s)

In the U.S.


  • Adderall

  • Adderall XR

Available Dosage Forms:


  • Tablet

  • Capsule, Extended Release

Therapeutic Class: CNS Stimulant


Chemical Class: Amphetamine


Uses For Adderall


Amphetamine and dextroamphetamine combination belongs to the group of medicines called central nervous system (CNS) stimulants. It is used to treat attention-deficit hyperactivity disorder (ADHD) and narcolepsy (uncontrollable desire for sleep or sudden attacks of deep sleep) .


Amphetamine and dextroamphetamine combination increases attention and decreases restlessness in patients who are overactive, cannot concentrate for very long or are easily distracted, and have unstable emotions. It is also used as part of a total treatment program that also includes social, educational, and psychological treatment .


Amphetamine and dextroamphetamine combination may also be used for other conditions as determined by your doctor .


This medicine is available only with a doctor's prescription. Prescriptions cannot be refilled. A new prescription must be obtained from your doctor each time you or your child needs this medicine .


Before Using Adderall


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of amphetamine and dextroamphetamine combination in children with attention-deficit hyperactivity disorder below 3 years of age. Safety and efficacy have not been established .


Geriatric


Appropriate studies on the relationship of age to the effects of amphetamine and dextroamphetamine combination have not been performed in the geriatric population .


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


Studies in women breastfeeding have demonstrated harmful infant effects. An alternative to this medication should be prescribed or you should stop breastfeeding while using this medicine.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. When you are taking this medicine, it is especially important that your healthcare professional know if you are taking any of the medicines listed below. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Using this medicine with any of the following medicines is not recommended. Your doctor may decide not to treat you with this medication or change some of the other medicines you take.


  • Clorgyline

  • Furazolidone

  • Iproniazid

  • Isocarboxazid

  • Moclobemide

  • Nialamide

  • Pargyline

  • Phenelzine

  • Procarbazine

  • Rasagiline

  • Selegiline

  • Sibutramine

  • Toloxatone

  • Tranylcypromine

Using this medicine with any of the following medicines is usually not recommended, but may be required in some cases. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Chlorpromazine

  • Citalopram

  • Furazolidone

  • Venlafaxine

Using this medicine with any of the following medicines may cause an increased risk of certain side effects, but using both drugs may be the best treatment for you. If both medicines are prescribed together, your doctor may change the dose or how often you use one or both of the medicines.


  • Guanethidine

Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. The following interactions have been selected on the basis of their potential significance and are not necessarily all-inclusive.


Other Medical Problems


The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:


  • Agitation, anxiety, or tension or

  • Arteriosclerosis (hardening of the arteries), severe or

  • Drug abuse or dependence, history of or

  • Glaucoma or

  • Heart disease or

  • High blood pressure, moderate to severe or

  • Overactive thyroid—This medicine should not be used in patients with these conditions .

  • Heart problems or defects or

  • High blood pressure, mild or

  • Mental illness (e.g., aggressive behavior, hostility, psychosis, mania, family history of suicide, bipolar illness, depression) or

  • Seizures, history of or

  • Thyroid problems—Use with caution. Serious side effects may occur .

  • Tourette's syndrome, history of or other tics—Children and their families should be checked by their doctor for this condition before taking this medicine .

Proper Use of amphetamine and dextroamphetamine

This section provides information on the proper use of a number of products that contain amphetamine and dextroamphetamine. It may not be specific to Adderall. Please read with care.


Take this medicine only as directed by your doctor. Do not take more or less of it, do not take it more often, and do not take it for a longer time than your doctor ordered. If too much is taken, it may become habit-forming (causing mental or physical dependence) .


If you think this medicine is not working properly after you have taken it for several weeks, do not increase the dose. Instead, check with your doctor .


This medicine should come with a Medication Guide. Read and follow these instructions carefully. Ask your doctor if you have any questions .


Swallow the extended-release capsule whole with water or other liquids. If you cannot swallow the extended-release capsule, you may open it and sprinkle the medicine into a small amount of applesauce. Stir this mixture well and swallow it right away without chewing. Do not store this mixture for future use. Do not crush or chew the medicine inside the capsule .


You may take the extended-release capsule with or without food .


Dosing


The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.


The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.


  • For oral dosage form (tablets):
    • For attention-deficit hyperactivity disorder:
      • Adults and children 6 years of age and older—At first, 5 milligrams (mg) one to two times a day. Your doctor may increase your dose if needed.

      • Children 3 to 5 years of age—At first, 2.5 mg daily. Your doctor may increase your dose if needed.

      • Children younger than 3 years of age—Use is not recommended .


    • For narcolepsy:
      • Adults, teenagers, and children 12 years of age and older—At first, 10 mg daily. Your doctor may adjust your dose if needed.

      • Children 6 to 12 years of age—At first, 5 mg daily. Your doctor may increase your dose if needed.

      • Children younger than 6 years of age—Dose must be determined by your doctor .



  • For oral dosage form (extended-release capsules):
    • For attention-deficit hyperactivity disorder:
      • Adults—20 milligrams (mg) once a day in the morning.

      • Children and teenagers 6 to 17 years of age—At first, 10 milligrams (mg) once a day in the morning. Your doctor may adjust your dose if needed.

      • Children younger than 6 years of age—Dose must be determined by your doctor .



Missed Dose


If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.


Storage


Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.


Keep out of the reach of children.


Do not keep outdated medicine or medicine no longer needed.


Ask your healthcare professional how you should dispose of any medicine you do not use.


Precautions While Using Adderall


It is very important that your doctor check your progress at regular visits to make sure this medicine is working properly and to check for unwanted effects .


If you will be taking this medicine in large doses for a long time, do not stop taking it without first checking with your doctor. Your doctor may want you to reduce gradually the amount you are taking before stopping completely .


Do not take this medicine within 14 days of taking an MAO inhibitor such as Eldepryl®, Marplan®, Nardil®, or Parnate®.


This medicine may cause some people to feel a false sense of well-being or to become dizzy, lightheaded, or less alert than they are normally. Make sure you know how you react to this medicine before you drive, use machines, or do anything else that could be dangerous if you are dizzy or are not alert.


Check with your doctor immediately if blurred vision, difficulty in reading, or any other change in vision occurs during or after treatment. Your doctor may want you to have your eyes checked by an ophthalmologist (eye doctor) .


If you have been using this medicine for a long time and you think you may have become mentally or physically dependent on it, check with your doctor. Some signs of dependence on amphetamines are:


  • A strong desire or need to continue taking the medicine.

  • A need to increase the dose to receive the effects of the medicine.

  • Withdrawal effects (for example, mental depression, nausea or vomiting, stomach cramps or pain, trembling, unusual tiredness or weakness) occurring after the medicine is stopped .

This medicine may cause slow growth. If your child is using this medicine, the doctor will need to keep track of your child's height and weight to make sure that your child is growing properly .


Do not take other medicines unless they have been discussed with your doctor. This includes prescription or nonprescription (over-the-counter [OTC]) medicines and herbal or vitamin supplements .


Before you have any medical tests, tell the medical doctor in charge that you are taking this medicine. The results of some tests may be affected by this medicine .


Adderall Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor immediately if any of the following side effects occur:


More common
  • Bladder pain

  • bloody or cloudy urine

  • difficult, burning, or painful urination

  • fast, pounding, or irregular heartbeat or pulse

  • frequent urge to urinate

  • lower back or side pain

Less common
  • Cold flu-like symptoms

  • cough or hoarseness

  • fever or chills

Incidence not known
  • Blistering, peeling, loosening of skin

  • chest pain or discomfort

  • confusion

  • convulsions

  • diarrhea

  • difficulty breathing

  • difficulty in speaking

  • difficulty swallowing

  • dizziness

  • double vision

  • faintness

  • hallucinations (seeing, hearing, or feeling things that are not there)

  • headache

  • inability to move arms, legs, or facial muscles

  • inability to speak

  • itching

  • joint or muscle pain

  • large, hive-like swelling on face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

  • loss of bladder control

  • muscle spasm or jerking of all extremities

  • nausea

  • pain or discomfort in arms, jaw, back, or neck

  • red irritated eyes

  • red skin lesions, often with a purple center

  • severe mental changes

  • shortness of breath

  • skin rash

  • slow speech

  • sore throat

  • sores, ulcers, or white spots in mouth or on lips

  • sudden loss of consciousness

  • sweating

  • swelling of feet or lower legs

  • tightness in chest

  • troubled breathing

  • uncontrolled vocal outbursts and/or tics (uncontrolled repeated body movements)

  • unusual tiredness or weakness

  • vomiting

  • wheezing

Get emergency help immediately if any of the following symptoms of overdose occur:


Symptoms of overdose
  • Blurred vision

  • dark-colored urine

  • discouragement

  • dizziness, faintness, or lightheadedness when getting up from a lying or sitting position suddenly

  • feeling sad or empty

  • irritability

  • lack of appetite

  • loss of interest or pleasure

  • muscle cramps or spasms

  • muscle pain or stiffness

  • nervousness

  • overactive reflexes

  • physical attempt to injure

  • restlessness

  • stomach cramps

  • trembling or shaking of legs, arms, hands, or feet

  • trouble concentrating

  • trouble sleeping

  • violent actions

  • panic state

  • pounding in the ears

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Anxiety

  • dry mouth

  • lack or loss of strength

  • sleeplessness

  • stomach pain

  • unable to sleep

  • weight loss

Incidence not known
  • Constipation

  • decreased interest in sexual intercourse

  • false or unusual sense of well-being

  • inability to have or keep an erection

  • loss in sexual ability, desire, drive, or performance

  • twitching, twisting, uncontrolled repetitive movements of tongue, lips, face, arms, or legs

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: Adderall side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More Adderall resources


  • Adderall Side Effects (in more detail)
  • Adderall Use in Pregnancy & Breastfeeding
  • Drug Images
  • Adderall Drug Interactions
  • Adderall Support Group
  • 108 Reviews for Adderall - Add your own review/rating


  • Adderall Prescribing Information (FDA)

  • Adderall Monograph (AHFS DI)

  • Adderall Consumer Overview

  • Adderall MedFacts Consumer Leaflet (Wolters Kluwer)

  • Adderall XR Prescribing Information (FDA)

  • Adderall XR Extended-Release Capsules MedFacts Consumer Leaflet (Wolters Kluwer)



Compare Adderall with other medications


  • ADHD
  • Narcolepsy

Forceval Capsules (Alliance Pharmaceuticals)





1. Name Of The Medicinal Product



Forceval Capsules


2. Qualitative And Quantitative Composition



Each capsule contains:











































































Vitamin A (as β-Carotene)

HSE

2,500.0 iu

Vitamin D2 (Ergocalciferol)

HSE

400.0 iu

Vitamin B1 (Thiamine)

USP

1.2 mg

Vitamin B2 (Riboflavin)

BP

1.6 mg

Vitamin B6 (Pyridoxine)

BP

2.0 mg

Vitamin B12 (Cyanocobalamin)

PhEur

3.0 mcg

Vitamin C (Ascorbic Acid)

BP

60.0 mg

Vitamin E (dl-α-Tocopheryl Acetate)

USP

10.0 mg

d-Biotin (Vitamin H)

FCC

100.0 mcg

Nicotinamide (Vitamin B3)

BP

18.0 mg

Pantothenic Acid (Vitamin B5)

USP

4.0 mg

Folic Acid (Vitamin B Complex)

BP

400.0 mcg

Calcium

FCC

100.0 mg

Iron

BP

12.0 mg

Copper

HSE

2.0 mg

Phosphorus

HSE

77.0 mg

Magnesium

BP

30.0 mg

Potassium

HSE

4.0 mg

Zinc

HSE

15.0 mg

Iodine

BP

140.0 mcg

Manganese

HSE

3.0 mg

Selenium

BP

50.0 mcg

Chromium

HSE

200.0 mcg

Molybdenum

HSE

250.0 mcg


3. Pharmaceutical Form



Brown and maroon, oblong, soft gelatin capsule printed with FORCEVAL in white on one side and with 6377 in white on the other side.



4. Clinical Particulars



4.1 Therapeutic Indications



1. As a therapeutic nutritional adjunct where the intake of vitamins and minerals is suboptimal, e.g. in the presence of organic disease such as malignancy and immune deficiency syndromes, such as AIDS.



2. As a therapeutic nutritional adjunct in conditions where the absorption of vitamins and minerals is suboptimal, e.g. malabsorption, inflammatory bowel disease and fistulae, short bowel syndrome and Crohn's disease, and where concurrent medication decreases vitamin and mineral absorption.



3. As a therapeutic nutritional adjunct in convalescence from illness, e.g. where anorexia or cachexia exists and following chemo- or radio-therapy.



4. As a therapeutic nutritional adjunct in convalescence from surgery, e.g. where nutritional intake continues to be inadequate.



5. As a therapeutic nutritional adjunct for patients on special or restricted diets, e.g. in renal diets and where several food groups are restricted in therapeutic weight reducing diets.



6. As a therapeutic nutritional adjunct where food intolerance exists, e.g. exclusion diets.



7. As an adjunct in synthetic diets, e.g. in phenylketonuria, galactosaemia and ketogenic diets.



4.2 Posology And Method Of Administration



Adults and the Elderly



One capsule daily, preferably taken one hour after meals. Do not exceed the stated dose. The capsule should be swallowed whole with water.



Children under 12 years of age



Forceval Capsules are not recommended for this age group.



4.3 Contraindications



Hypercalcaemia, haemochromatosis and other iron storage disorders.



4.4 Special Warnings And Precautions For Use



Whilst taking Forceval Capsules both protein and energy are also required to provide complete nutrition in the daily diet. No other vitamins, minerals or supplements with or without vitamin A should be taken with this preparation except under medical supervision.



Do not take Forceval Capsules on an empty stomach. Do not exceed the stated dose. Keep out of the reach of children. If symptoms persist, consult your doctor.



Important warning: Contains iron. Keep out of the reach and sight of children, as overdose may be fatal.



This medicine contains E123 (amaranth) and E124 (ponceau 4R red) which may cause allergic reactions.



Evidence from Randomised Control Trials suggests that high doses (20-30 mg/day) b-carotene intake may increase the risk of lung cancer in current smokers and those previously exposed to asbestos. This high-risk population should consider the potential risks and benefits of Forceval Capsules, which contain 4.5mg per recommended daily dose, before use.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



Folic acid can reduce the plasma concentration of phenytoin. Oral iron and zinc sulphate reduce the absorption of tetracyclines.



4.6 Pregnancy And Lactation



Forceval Capsules may be administered during pregnancy and lactation at the recommendation of the physician.



4.7 Effects On Ability To Drive And Use Machines



None anticipated.



4.8 Undesirable Effects



No undesirable effects due to Forceval therapy have been reported and none can be expected if the dosage schedule is adhered to.



4.9 Overdose



No cases of overdosage due to Forceval therapy have been reported. Any symptoms which may be observed due to the ingestion of large quantities of Forceval capsules will be due to the fat soluble vitamin content. If iron overdosage is suspected, symptoms may include nausea, vomiting, diarrhoea, abdominal pain, haematemesis, rectal bleeding, lethargy and circulatory collapse. Hyperglycaemia and metabolic acidosis may also occur. Treatment should be implemented immediately. In severe cases, after a latent phase, relapse may occur after 24 - 48 hours, manifest by hypotension coma and hepatocellular necrosis and renal failure.



Treatment



The following steps are recommended to minimise or prevent further absorption of the medication:



1. Administer an emetic.



2. Gastric lavage may be necessary to remove drug already released into the stomach. This should be undertaken using desferrioxamine solution (2 g/l). Desferrioxamine 5 g in 50 - 100 ml water should be introduced into the stomach following gastric emptying. Keep the patient under constant surveillance to detect possible aspiration of vomitus; maintain suction apparatus and standby emergency oxygen in case of need.



3. A drink of mannitol or sorbitol should be given to induce small bowel emptying.



4. Severe poisoning: in the presence of shock and/or coma with high serum iron levels (>142 μmol/l) immediate supportive measures plus i.v. infusion of desferrioxamine should be instituted. The recommended dose of desferrioxamine is 5 mg/kg/h by slow i.v. infusion up to a maximum of 80 mg/kg/24 hours. Warning: hypotension may occur if the infusion rate is too rapid.



5. Less severe poisoning: i.m. desferrioxamine 50 mg/kg up to a maximum dose of 4 g should be given.



6. Serum iron levels should be monitored throughout.



7. Any fluid or electrolyte imbalance should be corrected.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



The following account summarises the pharmacological effects of the vitamins and minerals in Forceval Capsules and describes the conditions caused by deficiency of these.



Vitamin A



Vitamin A plays an important role in the visual process. It is isomerised to the 11-cis isomer and subsequently bound to the opsin to form the photoreceptor for vision under subdued light. One of the earliest symptoms of deficiency is night blindness which may develop into the more serious condition xerophthalmia. Vitamin A also participates in the formation and maintenance of the integrity of epithelial tissues and mucous membranes. Deficiency may cause skin changes resulting in a dry rough skin with lowered resistance to minor skin infections. Deficiency of Vitamin A, usually accompanied by protein-energy malnutrition, is linked with a frequency of infection and with defective immunological defence mechanisms.



Vitamin D



Vitamin D is required for the absorption of calcium and phosphate from the gastro-intestinal tract and for their transport. Its involvement in the control of calcium metabolism and hence the normal calcification of bones is well documented. Deficiency of Vitamin D in children may result in the development of rickets.



Vitamin B1 (Thiamine)



Thiamine (as the coenzyme, thiamine pyrophosphate) is associated with carbohydrate metabolism. Thiamine pyrophosphate also acts as a co



Vitamin B2 (Riboflavine)



Riboflavine is phosphorylated to flavine mononucleotide and flavine adenine dinucleotide which act as co-enzymes in the respiratory chain and in oxidative phosphorylation. Riboflavine deficiency presents with ocular symptoms, as well as lesions on the lips and at angles of the mouth.



Vitamin B6 (Pyridoxine)



Pyridoxine, once absorbed, is rapidly converted to the co-enzymes pyridoxal phosphate and pyridoxamine phosphate which play an essential role in protein metabolism. Convulsions and hypochromic anaemia have occurred in infants deficient in pyridoxine.



Vitamin B12 (Cyanocobalamin)



Vitamin B12 is present in the body mainly as methylcobalamin and as adenosylcobalamin and hydroxocobalamin. These act as co-enzymes in the trans methylation of homocysteine to methionine; in the isomerisation of methylmalonyl co12 interferes with haemopoiesis and produces megaloblastic anaemia.



Vitamin C (Ascorbic Acid)



Vitamin C cannot be synthesised by man therefore a dietary source is necessary. It acts as a cofactor in numerous biological processes including the hydroxylation of proline to hydroxyproline. In deficiency, the formation of collagen is, therefore, impaired. Ascorbic acid is important in the hydroxylation of dopamine to noradrenaline and in hydroxylations occurring in steroid synthesis in the adrenals. It is a reducing agent in tyrosine metabolism and by acting as an electron donor in the conversion of folic acid to tetrahydrofolic acid is indirectly involved in the synthesis of purine and thymine. Vitamin C is also necessary for the incorporation of iron into ferritin. Vitamin C increases the phagocytic function of leucocytes; it possesses anti-inflammatory activity and it promotes wound healing. Deficiency can produce scurvy. Features include swollen inflamed gums, petechial haemorrhages and subcutaneous bruising. The deficiency of collagen leads to development of thin watery ground substances in which blood vessels are insecurely fixed and readily ruptured. The supportive components of bone and cartilage are also deficient causing bones to fracture easily and teeth to become loose. Anaemia commonly occurs probably due to Vitamin C's role in iron metabolism.



Vitamin E



Vitamin E deficiency has been linked to disorders such as cystic fibrosis where fat absorption is impaired. It is essential for the normal function of the muscular system and the blood.



Nicotinamide



The biochemical functions of nicotinamide as NAD and NADP (nicotinamide adenine dinucleotide phosphate) include the degradation and synthesis of fatty acids, carbohydrates and amino acids as well as hydrogen transfer. Deficiency produces pellagra and mental neurological changes.



Calcium (Dicalcium Phosphate)



Calcium is an essential body electrolyte. It is involved in the maintenance of normal muscle and nerve function and essential for normal cardiac function and the clotting of blood. Calcium is mainly found in the bones and teeth. Deficiency of calcium leads to rickets, osteomalacia in children and osteoporosis in the elderly.



Phosphorus (Dicalcium Phosphate)



Phosphate plays important roles in the osteoblastic and osteoclastic reactions. It interacts with calcium to modify the balance between these two processes. Organic phosphate esters play a key role in the metabolism of carbohydrates, fats and proteins and in the formation of 'high energy phosphate' compounds. Phosphate also acts as a buffer and plays a role in the renal excretion of sodium and hydrogen ions.



Pantothenic Acid



Pantothenic acid is incorporated into co-enzyme A and is involved in metabolic pathways involving acetylation which includes detoxification of drug molecules and biosynthesis of cholesterol, steroid hormones, mucopolysaccharides and acetylcholine. CoA has an essential function in lipid metabolism.



Folic Acid



Folic acid is reduced in the body to tetrahydrofolate which is a co-enzyme for various metabolic processes, including the synthesis of purine and pyrimidine nucleotides and hence in the synthesis of DNA. It is also involved in some amino acid conversion and in the formation and utilisation of formate. Deficiency of folic acid leads to megaloblastic anaemia.



Vitamin H (d-Biotin)



Biotin is a co-enzyme for carboxylation during the metabolism of proteins and carbohydrates.



Selenium



Selenium is an essential trace element, deficiency of which has been reported in man. It is thought to be involved in the functioning of membranes and the synthesis of amino acids. Deficiency of selenium in the diet of experimental animals produces fatty liver followed by necrosis.



Iron



Iron, as a constituent of haemoglobin, plays an essential role in oxygen transport. It is also present in the muscle protein myoglobin and in the liver. Deficiency of iron leads to anaemia.



Copper (Copper Sulphate)



Traces of copper are essential to the body as constituents of enzyme systems involved in oxidation reactions.



Magnesium (Magnesium Oxide)



Magnesium is essential to the body as a constituent of skeletal structures and in maintaining cell integrity and fluid balance. It is utilised in many of the functions in which calcium is concerned but often exerts the opposite effect. Some enzymes require the magnesium ion as a co-factor.



Potassium (Potassium Sulphate)



Potassium is the principle cation of intracellular fluid and is intimately involved in the cell function and metabolism. It is essential for carbohydrate metabolism and glycogen storage and protein synthesis and is involved in transmembrane potential where it is necessary to maintain the resting potential in excitable cells. Potassium ions maintain intracellular pH and osmotic pressure. Prolonged or severe diarrhoea may lead to potassium deficiency.



Zinc (Zinc Sulphate)



Zinc is a constituent of many enzymes and is, therefore, essential to the body. It is present with insulin in the pancreas. It plays a role in DNA synthesis and cell division. Reported effects of deficiency include delayed puberty and hypogonadal dwarfism.



Manganese (Manganese Sulphate)



Manganese is a constituent of enzyme systems including those involved in lipid synthesis, the tricarboxylic acid cycle and purine and pyrimidine metabolism. It is bound to arginase of the liver and activates many enzymes.



Iodine (Potassium Iodide)



Iodine is an essential constituent of the thyroid hormones.



Chromium (Chromium Amino Acid Chelate 10%)



Chromium is an essential trace element involved in carbohydrate metabolism.



Molybdenum (Sodium Molybdate)



Molybdenum is an essential trace element although there have been no reports of deficiency states in man. Molybdenum salts have been used to treat copper poisoning in sheep.



5.2 Pharmacokinetic Properties



The following account describes the absorption and fate of each of the active constituents of Forceval Capsules.



Vitamin A



Except when liver function is impaired, Vitamin A is readily absorbed. β



Vitamin D



The metabolism of ergocalciferol is similar to that of cholecalciferol. Cholecalciferol is absorbed from the gastro-intestinal tract into the circulation. In the liver, it is hydroxylated to 25-hydroxycholecalciferol, is subject to entero-hepatic circulation and is further hydroxylated to 1,25



Vitamin B1 (Thiamine)



Thiamine is absorbed from the gastro-intestinal tract and is widely distributed to most body tissues. Amounts in excess of the body's requirements are not stored but excreted in the urine as unchanged thiamine or its metabolites.



Vitamin B2 (Riboflavine)



Riboflavine is absorbed from the gastro-intestinal tract and in the circulation is bound to plasma proteins. It is widely distributed. Little is stored and excess amounts are excreted in the urine. In the body riboflavine is converted to flavine mononucleotide (FMN) and then to flavine adenine dinucleotide (FAD).



Vitamin B6 (Pyridoxine)



Pyridoxine is absorbed from the gastro-intestinal tract and converted to the active pyridoxal phosphate which is bound to plasma proteins. It is excreted in the urine as 4



Vitamin B12 (Cyanocobalamin)



Cyanocobalamin is absorbed from the gastro-intestinal tract and is extensively bound to specific plasma proteins. A study with labelled Vitamin B12 showed it was quickly taken up by the intestinal mucosa and held there for 2



Vitamin C (Ascorbic Acid)



Ascorbic acid is readily absorbed from the gastro-intestinal tract and is widely distributed in the body tissues. Ascorbic acid in excess of the body's needs is rapidly eliminated in the urine and this elimination is usually accompanied by a mild diuresis.



Vitamin E



Vitamin E is absorbed from the gastro-intestinal tract. Most appears in the lymph and is then widely distributed to all tissues. Most of a dose is slowly excreted in the bile and the remainder is eliminated in the urine as glucuronides of tocopheronic acid or other metabolites.



Nicotinamide (Nicotinic Acid Amide)



Nicotinic acid is absorbed from the gastro-intestinal tract, is widely distributed in the body tissues and has a short half-life.



Calcium (Dicalcium Phosphate)



A third of ingested calcium is absorbed from the small intestine. Absorption of calcium decreases with age.



Phosphorus (Dicalcium Phosphate)



The body contains from 600 - 800 g of phosphorus, over 80% of which is present in the bone as phosphate salts, mainly hydroxyapatite crystals. The phosphate in these crystals is available for exchange with phosphate ions in the extra-cellular fluids.



Calcium Pantothenate



Pantothenic acid is readily absorbed from the gastro-intestinal tract and is widely distributed in the body tissues. About 70% of pantothenic acid is excreted unchanged in the urine and about 30% in the faeces.



Folic Acid



Folic acid is absorbed mainly from the proximal part of the small intestine. Folate polyglutamates are considered to be deconjugated to monoglutamates during absorption. Folic acid rapidly appears in the blood where it is extensively bound to plasma proteins. Some folic acid is distributed in body tissues, some is excreted as folate in the urine and some is stored in the liver as folate.



Vitamin H (d-Biotin)



Following absorption, biotin is stored in the liver, kidney and pancreas.



Selenium



Although it has been established that selenium is essential to human life, very little information is available on its function and metabolism.



Ferrous Fumarate (Iron)



Iron is absorbed chiefly in the duodenum and jejunum. Absorption is aided by the acid secretion of the stomach and if the iron is in the ferrous state as in ferrous fumarate. In conditions of iron deficiency, absorption is increased and, conversely, it is decreased in iron overload. Iron is stored as ferritin.



Copper Sulphate (Copper)



Copper is absorbed from the gastro-intestinal tract and its major route of excretion is in the bile.



Magnesium Oxide (Magnesium)



Magnesium salts are poorly absorbed from the gastro-intestinal tract; however, sufficient magnesium will normally be absorbed to replace deficiency states. Magnesium is excreted in both the urine and the faeces but excretion is reduced in deficiency states.



Potassium Sulphate (Potassium)



Potassium salts are absorbed from the gastro-intestinal tract. Potassium is excreted in the urine, the faeces and in perspiration. Urinary excretion of potassium continues even when intake is low.



Zinc Sulphate (Zinc)



Zinc is poorly absorbed from the gastro-intestinal tract. It is widely distributed throughout the body. It is excreted in the faeces with traces appearing in the urine.



Manganese Sulphate (Manganese)



Manganese salts are poorly absorbed.



Potassium Iodide (Iodine)



Iodides are absorbed and stored in the thyroid gland as thyroglobulin. Iodides are excreted in the urine with smaller amounts appearing in the faeces, saliva and sweat.



Chromium Amino Acid Chelate 10% (Chromium)



Although it has been established that chromium is essential to human life, little information is available on its function and metabolism.



Sodium Molybdate (Molybdenum)



Although it has been established that molybdenum is essential to human life, little information is available on its function and metabolism.



5.3 Preclinical Safety Data



There are no pre-clinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.



6. Pharmaceutical Particulars



6.1 List Of Excipients



























Soya Bean Oil

BP

Soya Lecithin

HSE

Hard Vegetable Fat (Biscuitine 621)

HSE

Yellow Beeswax

BP

Purified Water

PhEur

Gelatin

BP

Glycerine

BP

Ponceau 4R (E124)

HSE

Amaranth (E123)

HSE

Titanium Dioxide (E171)

BP

Red Iron Oxide Paste (E172)

HSE

Vegetable Black Paste (E153)

HSE


6.2 Incompatibilities



No major incompatibilities are known.



6.3 Shelf Life



24 months, as packaged for sale.



6.4 Special Precautions For Storage



Store in a cool dry place at a temperature not exceeding 25°C.



Protect from light.



6.5 Nature And Contents Of Container



The product is presented in press-thru blister packs, each blister strip containing 15 Forceval capsules. The blister strip is composed of PVC/PVdC with a printed aluminium foil lidding. The foil is printed (red on gold) with the name and PL number of the product, the number of vitamins and minerals per capsule and the daily dose.



The product is available in packs of 15, 30, 45 or 90 capsules.



6.6 Special Precautions For Disposal And Other Handling



Not applicable.



7. Marketing Authorisation Holder



Alliance Pharmaceuticals Ltd



Avonbridge House



2 Bath Road



Chippenham



Wiltshire



SN15 2BB



United Kingdom



8. Marketing Authorisation Number(S)



PL 16853/0079



9. Date Of First Authorisation/Renewal Of The Authorisation



30/11/2005



10. Date Of Revision Of The Text



14/02/2007




Sunday, 1 July 2012

Boots Bite and Sting Relief Antihistamine Cream / Boots Bite and Sting Relief 2 Years Plus Antihistamine Cream





1. Name Of The Medicinal Product



Bite and Sting Relief Antihistamine Cream


2. Qualitative And Quantitative Composition








 




% quantity




Mepyramine maleate, Ph Eur




2.0% w/w



3. Pharmaceutical Form



Cream.



4. Clinical Particulars



4.1 Therapeutic Indications



P: For the symptomatic relief of insect bites and stings and nettle rash.



GSL: For the symptomatic relief of insect bites and stings and nettle stings.



4.2 Posology And Method Of Administration



P: For adults, children and the elderly: Rub gently on to the affected area sparingly two or three times each day for up to three days.



GSL: For adults, elderly and children 2 years of age and over: Rub gently on to the affected area sparingly two or three times each day for up to three days.



For topical application to the skin.



4.3 Contraindications



Hypersensitivity to any of the ingredients or other antihistamines.



Should not be applied to acute vesicular and exudative dermatoses or eczema.



4.4 Special Warnings And Precautions For Use



P & GSL:



Do not apply to broken skin or eczema.



Not to be applied to large areas of skin.



If rash develops or gets worse stop using the product.



For external use only.



Keep all medicines out of the reach of children.



If symptoms do not go away, talk to your doctor.



In addition GSL:



Do not apply to sunburnt skin.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



No clinically significant drug interactions expected.



4.6 Pregnancy And Lactation



The safety of this product during pregnancy and lactation has not been established. In view of the potential for systemic absorption through the skin, the product should not be used during these periods unless under medical supervision.



4.7 Effects On Ability To Drive And Use Machines



No adverse effects known.



4.8 Undesirable Effects



Occasional local hypersensitivity reactions.



4.9 Overdose



In cases of excessive application to the skin, sufficient absorption may occur to give rise to systemic adverse effects. Treatment should be symptomatic.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Mepyramine maleate is an H1 receptor antagonist (antihistamine) of the ethylene diamine type. It diminishes or abolishes the effects of histamine in the body by competitive reversible blockade of histamine receptor sites on tissues.



5.2 Pharmacokinetic Properties



Mepyramine maleate is readily absorbed through the skin, metabolised in the liver and excreted, mainly as metabolites in the urine.



5.3 Preclinical Safety Data



There are no preclinical data of relevance to the prescriber which are additional to that already included.



6. Pharmaceutical Particulars



6.1 List Of Excipients



White soft paraffin BP



Liquid paraffin Ph Eur



Anhydrous lanolin EP



Arlacel 83 HSE



Cetomacrogol 1000 BP



Cetostearyl alcohol Ph Eur



Citric acid monohydrate Ph Eur



Sodium citrate Ph Eur



Purified water Ph Eur



6.2 Incompatibilities



None known.



6.3 Shelf Life



24 months.



6.4 Special Precautions For Storage



Do not store above 25°C.



6.5 Nature And Contents Of Container



A collapsible internally lacquered aluminium tube with membrane seal fitted with a high density polyethylene cap.



Pack size



P: 25gm, 30gm.



GSL: 20g



6.6 Special Precautions For Disposal And Other Handling



Not applicable.



7. Marketing Authorisation Holder



The Boots Company PLC



1 Thane Road West



Nottingham NG2 3AA



8. Marketing Authorisation Number(S)



PL 00014/0440



9. Date Of First Authorisation/Renewal Of The Authorisation



Date of first authorisation: 28 September 1993



Date of last renewal: 12 November 2003



10. Date Of Revision Of The Text



January 2005