Fipexiam may be available in the countries listed below.
Ampicillin is reported as an ingredient of Fipexiam in the following countries:
Sulbactam is reported as an ingredient of Fipexiam in the following countries:
Sultamicillin is reported as an ingredient of Fipexiam in the following countries:
International Drug Name Search
Dynexan Mundgel may be available in the countries listed below.
Lidocaine hydrochloride (a derivative of Lidocaine) is reported as an ingredient of Dynexan Mundgel in the following countries:
Lidocaine hydrochloride monohydrate (a derivative of Lidocaine) is reported as an ingredient of Dynexan Mundgel in the following countries:
Tetracaine hydrochloride (a derivative of Tetracaine) is reported as an ingredient of Dynexan Mundgel in the following countries:
International Drug Name Search
Amos Leva Korrel may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Levamisole hydrochloride (a derivative of Levamisole) is reported as an ingredient of Amos Leva Korrel in the following countries:
International Drug Name Search
Calmafen may be available in the countries listed below.
Ibuprofen is reported as an ingredient of Calmafen in the following countries:
International Drug Name Search
Pulmo-Timelets may be available in the countries listed below.
Theophylline is reported as an ingredient of Pulmo-Timelets in the following countries:
International Drug Name Search
Zolpidemtartraat A may be available in the countries listed below.
Zolpidem tartrate (a derivative of Zolpidem) is reported as an ingredient of Zolpidemtartraat A in the following countries:
International Drug Name Search
Lenar may be available in the countries listed below.
Omeprazole is reported as an ingredient of Lenar in the following countries:
International Drug Name Search
Emedyl may be available in the countries listed below.
Dimenhydrinate is reported as an ingredient of Emedyl in the following countries:
International Drug Name Search
Glycerin Suppositories may be available in the countries listed below.
Glycerol is reported as an ingredient of Glycerin Suppositories in the following countries:
International Drug Name Search
Triptilin may be available in the countries listed below.
Amitriptyline hydrochloride (a derivative of Amitriptyline) is reported as an ingredient of Triptilin in the following countries:
International Drug Name Search
Sodium sulfacetamide is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically sodium sulfacetamide is N-[(4-aminophenyl)sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is:
Each gram of ROSANIL® (sodium sulfacetamide 10% and sulfur 5%) Cleanser contains: Active: sodium sulfacetamide 10% (100 mg), sulfur 5% (50 mg). Inactive: butylated hydroxytoluene, edetate disodium, emulsifying wax, hydrochloric acid, light mineral oil, methylparaben, PPG-2 hydroxyethyl coco/isostearamide, propylparaben, purified water, sodium cocoyl isethionate, sodium lauryl sulfoacetate (and) disodium laureth sulfosuccinate, and sodium thiosulfate.
The most widely accepted mechanism of action of sulfonamides is the Woods-Fildes theory which is based on the fact that sulfonamides act as competitive antagonists to para-aminobenzoic acid (PABA), an essential component for bacterial growth. While absorption through intact skin has not been determined, sodium sulfacetamide is readily absorbed from the gastrointestinal tract when taken orally and excreted in the urine, largely unchanged. The biological half-life has variously been reported as 7 to 12.8 hours. The exact mode of action of sulfur in the treatment of acne is unknown, but it has been reported that it inhibits the growth of Propionibacterium acnes and the formation of free fatty acids.
ROSANIL® Cleanser is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
ROSANIL® Cleanser is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. ROSANIL® Cleanser is not to be used by patients with kidney disease.
Although rare, sensitivity to sodium sulfacetamide may occur. Therefore, caution and careful supervision should be observed when prescribing this drug for patients who may be prone to hypersensitivity to topical sulfonamides. Systemic toxic reactions such as agranulocytosis, acute hemolytic anemia, purpura hemorrhagica, drug fever, jaundice, and contact dermatitis indicate hypersensitivity to sulfonamides. Particular caution should be employed if areas of denuded or abraded skin are involved.
FOR EXTERNAL USE ONLY. Keep away from eyes. Keep out of reach of children. Keep container tightly closed.
General: If irritation develops, use of the product should be discontinued and appropriate therapy instituted. Patients should be carefully observed for possible local irritation or sensitization during long-term therapy. The object of this therapy is to achieve desquamation without irritation, but sodium sulfacetamide and sulfur can cause reddening and scaling of the epidermis. These side effects are not unusual in the treatment of acne vulgaris, but patients should be cautioned about the possibility.
Information for Patients: Avoid contact with eyes, eyelids, lips and mucous membranes. If accidental contact occurs, rinse with water. If excessive irritation develops, discontinue use and consult your physician.
Carcinogenesis, Mutagenesis and Impairment of Fertility: Long-term studies in animals have not been performed to evaluate carcinogenic potential.
Pregnancy: Category C. Animal reproduction studies have not been conducted with ROSANIL® (sodium sulfacetamide 10% and sulfur 5%) Cleanser. It is also not known whether ROSANIL® Cleanser can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. ROSANIL® Cleanser should be given to a pregnant woman only if clearly needed.
Nursing Mothers: It is not known whether sodium sulfacetamide is excreted in the human milk following topical use of ROSANIL® Cleanser. However, small amounts of orally administered sulfonamides have been reported to be eliminated in human milk. In view of this and because many drugs are excreted in human milk, caution should be exercised when ROSANIL® Cleanser is administered to a nursing woman.
Pediatric Use: Safety and effectiveness in children under the age of 12 have not been established.
Although rare, sodium sulfacetamide may cause local irritation.
Wash affected areas once or twice daily, or as directed by your physician. Avoid contact with eyes or mucous membranes. Wet skin and liberally apply to areas to be cleansed, massage gently into skin for 10–20 seconds working into a full lather, rinse thoroughly and pat dry. If drying occurs, it may be controlled by rinsing cleanser off sooner or using less often.
ROSANIL® (sodium sulfacetamide 10% and sulfur 5%) Cleanser is available in a 6 oz tube.
NDC 0299-3839-06
Store at controlled room temperature 20° - 25°C (68° - 77°F).
Marketed by:
GALDERMA LABORATORIES, L.P.
Fort Worth, Texas 76177 USA
Manufactured by:
DPT Laboratories, Ltd.
San Antonio, Texas 78215 USA
GALDERMA is a registered trademark.
www.rosanil.com
325076-0706 Revised: July 2006
Rx only
NDC 0299-3839-06
Rosanil®
(sodium sulfacetamide10%, sulfur 5%)
CLEANSER
NET WT. 6 oz (170 g)
GALDERMA
INDICATIONS: For the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
DIRECTIONS: Wash affected areas once or twice daily, or as directed by your physician. Avoid contact with eyes or mucous membranes. Wet skin and liberally apply to areas to be cleansed, massage gently into skin for 10–20 seconds working into a full lather, rinse thoroughly and pat dry. If drying occurs, it may be controlled by rinsing cleanser off sooner or using less often.
WARNINGS: FOR EXTERNAL USE ONLY. Keep away from eyes. Keep out of reach of children. Keep tube tightly closed.
Each gram contains: ACTIVE: Sodium sulfacetamide 10% (100 mg), sulfur 5% (50 mg). INACTIVE: Butylated hydroxytoluene, edetate disodium, emulsifying wax, hydrochloric acid, light mineral oil, methylparaben, PPG-2 hydroxyethyl coco/isostearamide, propylparaben, purified water, sodium cocoyl isethionate, sodium lauryl sulfoacetate (and) disodium laureth sulfosuccinate, and sodium thiosulfate.
Store at controlled room temperature 20°-25°C (68°-77°F).
Lot number and expiration date on bottom of carton.
Marketed by:
GALDERMA LABORATORIES, L.P.
Fort Worth, Texas 76177 USA
Manufactured by:
DPT Laboratories, Ltd.
San Antonio, Texas 78215 USA
Galderma is a registered trademark.
www.rosanil.com
310100-1103
LOT:
EXP.:
| ROSANIL sodium sulfacetamide, sulfer solution | ||||||||||||||||||||||||||
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| Marketing Information | |||
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved drug other | 01/31/2003 | ||
| Labeler - Galderma Laboratories, L.P. (047350186) |
| Establishment | |||
| Name | Address | ID/FEI | Operations |
| DPT Laboratories, Ltd. | 832224526 | MANUFACTURE | |
Generic Name: lenalidomide (LEN a LID o mide)
Brand Names: Revlimid
Lenalidomide affects the immune system. It helps promote immune responses to prevent inflammation in the body.
Lenalidomide treats anemia (a lack of red blood cells in the body) and multiple myeloma (cancer resulting from a progressive blood disease). It is used in patients with myelodysplastic syndrome caused by an abnormal chromosome. This disorder is also called deletion 5q MDS, because part of chromosome 5 is missing. In people with this disorder, the bone marrow does not produce enough healthy blood cells.
Lenalidomide may also be used for other purposes not listed in this medication guide.
For Women: You will be required to use two reliable forms of birth control beginning 4 weeks before you start taking lenalidomide and ending 4 weeks after you stop taking it. Any woman who has not had a hysterectomy or has not been in menopause for at least 24 months in a row must agree in writing to use birth control before, during, and after taking lenalidomide. Even women with fertility problems are required to use birth control while taking this medication. You must also have a negative pregnancy test at 10 to 14 days before treatment and again at 24 hours before. While you are taking lenalidomide, you will have a pregnancy test every 4 weeks.
Stop using lenalidomide and call your doctor at once if you quit using birth control, if your period is late, or if you think you might be pregnant.
For Men: You must not cause a woman to become pregnant while you are taking lenalidomide because the medicine may affect your sperm and cause birth defects in the baby. You must agree in writing to always use latex condoms when having sex with a woman who is able to get pregnant, even if you have had a vasectomy.
Lenalidomide is available only under a special program called RevAssist. You must be registered in the program and sign documents stating that you understand the dangers of this medication and that you agree to use birth control measures as required by the program.
This medication comes with patient instructions for safe and effective use. Follow these directions carefully. Never give lenalidomide to another person, even if he or she has the same disorder for which you are being treated.
If you have certain conditions, you may need a dose adjustment or special tests to safely take this medication. Before taking lenalidomide, tell your doctor if you have:
a history of blood clots or stroke.
For Women: If you have not had a hysterectomy or have not been in menopause for at least 24 months in a row, you will be required to use two forms of birth control beginning 4 weeks before you start taking lenalidomide and ending 4 weeks after you stop taking it. Even women with fertility problems are required to use birth control while taking this medication. You must also have a negative pregnancy test at 10 to 14 days before treatment and again at 24 hours before. While you are taking lenalidomide, you will have a pregnancy test every 4 weeks.
The birth control method you use must be proven highly effective, such as birth control pills, an intrauterine device (IUD), a tubal ligation, or a sexual partner's vasectomy. The extra form of birth control you use must be a barrier method such as a latex condom, a diaphragm, or a cervical cap.
For Men: You must not cause a woman to become pregnant while you are taking lenalidomide because the medicine may affect your sperm and cause birth defects in the baby. You must agree in writing to always use latex condoms when having sex with a woman who is able to get pregnant, even if you have had a vasectomy. Contact your doctor if you have had unprotected sex, even once, or if you think your female sexual partner may be pregnant.
Lenalidomide is available only under a special program called RevAssist. Under this program, only registered doctors and pharmacists can prescribe and dispense lenalidomide. You must be registered in the program and sign documents stating that you understand the dangers of this medication and that you agree to use birth control measures as required by the program.
While you are using lenalidomide, you will be required to be listed on a patient registry and participate in occasional telephone surveys. You will be limited to a 28-day supply of lenalidomide each time your prescription is refilled. You may continue getting refills only if you participate fully in the RevAssist program and commit to all agreements.
Take this medication exactly as prescribed by your doctor. Do not take it in larger amounts or for longer than recommended. Follow the directions on your prescription label.
This medication comes with patient instructions for safe and effective use. Follow these directions carefully. Never give lenalidomide to another person, even if he or she has the same disorder for which you are being treated.
Your doctor may occasionally change your dose to make sure you get the best results from this medication.
Swallow the capsule whole, without breaking it open.
To be sure lenalidomide is helping your condition and not causing harmful effects, your blood will need to be tested every week for the first two months of treatment, and then every month after that. Do not miss any visits to your doctor.
Take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take only the next regularly scheduled dose. Do not take extra medicine to make up the missed dose.
An overdose of lenalidomide is not expected to produce life-threatening symptoms.
Call your doctor at once if you have any of these serious side effects:
chest pain, sudden shortness of breath, coughing up blood;
pain or swelling in your arm, thigh, or calf;
easy bruising, unusual bleeding or weakness;
fever, chills, body aches, flu symptoms;
lower back pain, blood in your urine;
urinating less than usual or not at all;
numbness or tingly feeling around your mouth;
muscle weakness, tightness, or contraction, overactive reflexes;
fast or slow heart rate, weak pulse, feeling short of breath, confusion, fainting;
severe blistering, peeling, and red skin rash; or
the first sign of any skin rash, no matter how mild.
Less serious side effects may include:
nausea, diarrhea, constipation;
dry or itchy skin;
runny or stuffy nose;
muscle or joint pain;
headache; or
tiredness.
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.
There may be other drugs that can affect lenalidomide. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.
See also: Revlimid side effects (in more detail)
Rec.INN
0099593-25-6
C21-H20-Cl2-N6-O3
475
Agent for premedication
Hypnotic and sedative agent
5-[(2-Aminoacetamido)methyl]-1-[4-chloro-2-(o-chlorobenzoyl)phenyl]-N,N-dimethyl-1H-1,2,4-triazole-3-carboxamide
International Drug Name Search
Glossary
| IS | Inofficial Synonym |
| JAN | Japanese Accepted Name |
| OS | Official Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Rhewlin may be available in the countries listed below.
Diclofenac sodium salt (a derivative of Diclofenac) is reported as an ingredient of Rhewlin in the following countries:
International Drug Name Search
Generic Name: permethrin topical (per METH rin)
Brand Names: Elimite, Lice Bedding Spray, Nix Complete Lice Treatment System, Nix Cream Rinse, Nix Lice Control, RID Home Lice Control Spray for Surfaces
Permethrin is an anti-parasite medication.
Permethrin topical (for the skin) is used to treat head lice and scabies.
Permethrin topical may also be used for other purposes not listed in this medication guide.
Use this medication exactly as directed on the label, or as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended.
Avoid sexual or intimate contact with others until your lice or scabies infection has cleared up. Avoid sharing hair brushes, combs, hair accessories, hats, clothing, bed linens, and other articles of personal use. Lice and scabies infections are highly contagious.
Use this medication exactly as directed on the label, or as prescribed by your doctor. Do not use it in larger amounts or for longer than recommended.
To treat scabies:
Make sure your skin is clean and dry. Apply a thin layer of permethrin topical to all body parts from the neck down to the soles of the feet. Rub in completely. Leave the medication on for 8 to 14 hours, then wash it off completely.
If your condition does not clear up within 14 days after applying permethrin topical, use another application.
To treat head lice:
When using the shampoo, apply it to dry hair only. Cover all hair completely and leave the shampoo in for 10 minutes. Then work into a lather using warm water and rinse out thoroughly.
When using the cream rinse, wash your hair using shampoo only (no conditioner or 2-in-1 shampoo). Rinse thoroughly and towel dry the hair, leaving it damp. Apply enough of the cream rinse to completely saturate all hair. Leave the cream rinse in your hair for 10 minutes.
Use a second application if lice are still seen 7 days after your first treatment.
You may also use a nit comb to remove lice eggs from the hair. Your hair should be slightly damp while using a nit comb. Work on only one section of hair at a time, combing through 1- to 2-inch strands from the scalp to the ends.
Rinse the nit comb often during use. Place removed nits into a sealed plastic bag and throw it into the trash to prevent re-infestation.
Check the scalp again daily to make sure all nits have been removed.
To treat pubic lice (crabs):
Wash and dry the treatment area. Apply permethrin topical to all pubic hair and any surrounding hairs on the thighs and around the anus.
Avoid getting this medication inside the rectum or vagina.
Leave the medication in for 10 minutes. Then work into a lather using warm water and rinse out thoroughly.
You may also use a nit comb to remove lice eggs from pubic hair (hair should be slightly damp).
All sexual partners should also be treated to prevent re-infestation of crabs.
Use permethrin surface spray to disinfect non-washable items such as:
furniture;
mattresses and pillows;
stuffed toys;
hats, gloves, and scarves;
headphones or headbands;
the inside of a bike helmet; or
seats and carpets inside your car.
Stuffed toys or pillows that cannot be washed should be sealed in air-tight plastic bags for 4 weeks.
Vacuum all rugs and carpets and throw away the vacuum cleaner bag.
Since permethrin topical is usually needed only once, you are not likely to be on a dosing schedule. Wait at least 7 days before using a second application.
Symptoms of a permethrin topical overdose are unknown.
Do not use other medicated skin products unless your doctor has told you to.
Avoid sexual or intimate contact with others until your lice or scabies infection has cleared up. Avoid sharing hair brushes, combs, hair accessories, hats, clothing, bed linens, and other articles of personal use. Lice and scabies infections are highly contagious.
Less serious side effects may include:
itching or mild skin rash;
mild burning, stinging, or redness; or
numbness or tingling where the medication was applied.
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.
It is not likely that other drugs you take orally or inject will have an effect on topically applied permethrin. But many drugs can interact with each other. Tell your doctor about all your prescription and over-the-counter medications, vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start a new medication without telling your doctor.
See also: RID Home Lice Control for Surfaces side effects (in more detail)
Roxatidine Acetate Hydrochloride may be available in the countries listed below.
Roxatidine Acetate Hydrochloride (BANM, JAN, USAN) is also known as Roxatidine (Rec.INN)
International Drug Name Search
Glossary
| BANM | British Approved Name (Modified) |
| JAN | Japanese Accepted Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Asalazin Medichrom may be available in the countries listed below.
Mesalazine is reported as an ingredient of Asalazin Medichrom in the following countries:
International Drug Name Search
Aspagin may be available in the countries listed below.
Tenoxicam is reported as an ingredient of Aspagin in the following countries:
International Drug Name Search
Celltaxel may be available in the countries listed below.
Paclitaxel is reported as an ingredient of Celltaxel in the following countries:
International Drug Name Search
In the US, Pentostatin (pentostatin systemic) is a member of the drug class antibiotics/antineoplastics and is used to treat Hairy Cell Leukemia.
US matches:
Rec.INN
L01XX08
0053910-25-1
C11-H16-N4-O4
268
Antineoplastic antibacterial
2'-Deoxycoformycin
Imidazo[4,5-d][1,3]diazepin-8-ol, 3-(2-deoxy-ß-D-erythro-pentofuranosyl)-3,6,7,8-tetrahydro-, (R)-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| DCF | Dénomination Commune Française |
| IS | Inofficial Synonym |
| JAN | Japanese Accepted Name |
| OS | Official Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Loseca may be available in the countries listed below.
Omeprazole is reported as an ingredient of Loseca in the following countries:
International Drug Name Search
Magnésium/Vitamine B6 Biogaran may be available in the countries listed below.
Magnesium Lactate dihydrate (a derivative of Magnesium Lactate) is reported as an ingredient of Magnésium/Vitamine B6 Biogaran in the following countries:
Pyridoxine hydrochloride (a derivative of Pyridoxine) is reported as an ingredient of Magnésium/Vitamine B6 Biogaran in the following countries:
International Drug Name Search
In the US, Betagan (levobunolol ophthalmic) is a member of the drug class ophthalmic glaucoma agents and is used to treat Glaucoma - Open Angle and Intraocular Hypertension.
US matches:
UK matches:
Levobunolol is reported as an ingredient of Betagan in the following countries:
Levobunolol hydrochloride (a derivative of Levobunolol) is reported as an ingredient of Betagan in the following countries:
International Drug Name Search
Glossary
| SPC | Summary of Product Characteristics (UK) |
Allerdryl may be available in the countries listed below.
Diphenhydramine hydrochloride (a derivative of Diphenhydramine) is reported as an ingredient of Allerdryl in the following countries:
International Drug Name Search
Losamet may be available in the countries listed below.
Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Losamet in the following countries:
International Drug Name Search
Olanzapin ratiopharm may be available in the countries listed below.
Olanzapine is reported as an ingredient of Olanzapin ratiopharm in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
Rec.INN
D07AB03,D07XB01
0002135-17-3
C22-H28-F2-O5
410
Adrenal cortex hormone, glucocorticoid
Pregna-1,4-diene-3,20-dione, 6,9-difluoro-11,17,21-trihydroxy-16-methyl-, (6α,11ß,16α)-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| BANM | British Approved Name (Modified) |
| DCF | Dénomination Commune Française |
| IS | Inofficial Synonym |
| JAN | Japanese Accepted Name |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Paraldéhyde may be available in the countries listed below.
Paraldéhyde (DCF) is known as Paraldehyde in the US.
International Drug Name Search
Glossary
| DCF | Dénomination Commune Française |
Osteogenon may be available in the countries listed below.
Hydroxyapatite is reported as an ingredient of Osteogenon in the following countries:
International Drug Name Search
Forthane may be available in the countries listed below.
Isoflurane is reported as an ingredient of Forthane in the following countries:
International Drug Name Search
Generic Name: calcium carbonate (KAL see um KAR boe nate)
Brand Names: Alka-Mints, Cal-Gest, Calcarb, Calci Mix, Calci-Chew, Calci-Mix, Calcium Concentrate, Calcium Liquid Softgel, Calcium Oyster Shell, Caltrate, Chooz, Extra Strength Mylanta Calci Tabs, Icar Prenatal Chewable Calcium, Maalox Antacid Barrier, Maalox Childrens', Maalox Quick Dissolve, Maalox Quick Dissolve Maximum Strength, Maalox Regular Strength, Mylanta Child, Nephro Calci, Os-Cal 500, Oysco 500, Oyst Cal 500, Oyster Cal, Oyster Calcium, Oyster Shell, Pepto Children's, Rolaids Sodium Free, Rolaids Soft Chew, Titralac, Tums, Tums 500, Tums E-X, Tums Kids, Tums QuikPak, Tums Ultra
Calcium is a mineral that is found naturally in foods. Calcium is necessary for many normal functions of the body, especially bone formation and maintenance. Calcium can also bind to other minerals (such as phosphate) and aid in their removal from the body.
Calcium carbonate is used to prevent and to treat calcium deficiencies.
Calcium carbonate may also be used for purposes not listed in this medication guide.
To make sure you can safely take calcium carbonate, tell your doctor if you have any of these other conditions:
a history of kidney stones; or
a parathyroid gland disorder.
Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.
The chewable tablet should be chewed before you swallow it.
Use the calcium carbonate powder as directed. Allow the powder to dissolve completely, then consume the mixture.
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.
Overdose symptoms may include nausea, vomiting, decreased appetite, constipation, confusion, delirium, stupor, and coma.
Follow your healthcare provider's instructions about any restrictions on food, beverages, or activity.
Less serious side effects may include:
nausea or vomiting;
decreased appetite;
constipation;
dry mouth or increased thirst; or
urinating more than usual.
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.
Calcium carbonate can make it harder for your body to absorb other medications you take by mouth. Tell your doctor if you are taking:
digoxin (Lanoxin, Lanoxicaps);
antacids or other calcium supplements;
calcitriol (Rocaltrol) or vitamin D supplements; or
doxycycline (Adoxa, Doryx, Oracea, Vibramycin), minocycline (Dynacin, Minocin, Solodyn, Vectrin), or tetracycline (Brodspec, Panmycin, Sumycin, Tetracap).
This list is not complete and other drugs may interact with calcium carbonate. 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.
See also: Oyster Calcium side effects (in more detail)
Fluoxetin AL may be available in the countries listed below.
Fluoxetine hydrochloride (a derivative of Fluoxetine) is reported as an ingredient of Fluoxetin AL in the following countries:
International Drug Name Search
Prevensyl may be available in the countries listed below.
Ramipril is reported as an ingredient of Prevensyl in the following countries:
International Drug Name Search
Zoroxin may be available in the countries listed below.
Norfloxacin is reported as an ingredient of Zoroxin in the following countries:
International Drug Name Search
Neptor may be available in the countries listed below.
Esomeprazole is reported as an ingredient of Neptor in the following countries:
International Drug Name Search
In the US, Sorbitrate is a member of the drug class antianginal agents and is used to treat Angina, Angina Pectoris Prophylaxis, Esophageal Spasm, Heart Failure and Pulmonary Arterial Hypertension.
Isosorbide Dinitrate is reported as an ingredient of Sorbitrate in the following countries:
International Drug Name Search
Normalax may be available in the countries listed below.
Lactulose is reported as an ingredient of Normalax in the following countries:
International Drug Name Search
Lignocaine Gel 2% may be available in the countries listed below.
Lidocaine hydrochloride (a derivative of Lidocaine) is reported as an ingredient of Lignocaine Gel 2% in the following countries:
International Drug Name Search
Simetyl may be available in the countries listed below.
Simeticone is reported as an ingredient of Simetyl in the following countries:
International Drug Name Search
Azrogen may be available in the countries listed below.
Lorazepam is reported as an ingredient of Azrogen in the following countries:
International Drug Name Search
Vitaminac R may be available in the countries listed below.
Ascorbic Acid is reported as an ingredient of Vitaminac R in the following countries:
International Drug Name Search
Ferromax may be available in the countries listed below.
Ferrous Sulfate is reported as an ingredient of Ferromax in the following countries:
International Drug Name Search
Buvasodil may be available in the countries listed below.
Buflomedil hydrochloride (a derivative of Buflomedil) is reported as an ingredient of Buvasodil in the following countries:
International Drug Name Search
Hipertex may be available in the countries listed below.
Captopril is reported as an ingredient of Hipertex in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
In the US, Dextromethorphan (dextromethorphan systemic) is a member of the drug class antitussives and is used to treat Cough.
US matches:
Prop.INN
R05DA09
0000125-71-3
C18-H25-N-O
271
Cough suppressant
Morphinan, 3-methoxy-17-methyl-, (9α,13α,14α)-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| BANM | British Approved Name (Modified) |
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| JAN | Japanese Accepted Name |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Prop.INN | Proposed International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
