Moxaclav may be available in the countries listed below.
Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Moxaclav in the following countries:
Clavulanic Acid potassium (a derivative of Clavulanic Acid) is reported as an ingredient of Moxaclav in the following countries:
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Gayabeksin may be available in the countries listed below.
Sulfogaiacol is reported as an ingredient of Gayabeksin in the following countries:
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Cohistan may be available in the countries listed below.
Chlorphenamine maleate (a derivative of Chlorphenamine) is reported as an ingredient of Cohistan in the following countries:
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Angitil may be available in the countries listed below.
UK matches:
Diltiazem hydrochloride (a derivative of Diltiazem) is reported as an ingredient of Angitil in the following countries:
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Glossary
| SPC | Summary of Product Characteristics (UK) |
In the US, Theo-Dur (theophylline systemic) is a member of the drug class methylxanthines and is used to treat Apnea of Prematurity, Asthma - acute and Asthma - Maintenance.
US matches:
Theophylline is reported as an ingredient of Theo-Dur in the following countries:
International Drug Name Search
T-Cef may be available in the countries listed below.
Cefixime is reported as an ingredient of T-Cef in the following countries:
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Quinine Bisulphate may be available in the countries listed below.
UK matches:
Quinine Bisulphate (BANM) is known as Quinine in the US.
International Drug Name Search
Glossary
| BANM | British Approved Name (Modified) |
| SPC | Summary of Product Characteristics (UK) |
Aciclovir EG may be available in the countries listed below.
Aciclovir is reported as an ingredient of Aciclovir EG in the following countries:
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Neulactil may be available in the countries listed below.
UK matches:
Periciazine is reported as an ingredient of Neulactil in the following countries:
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Glossary
| SPC | Summary of Product Characteristics (UK) |
Definition of Giardiasis: An infection of the small intestine caused by a protozoa,
The following drugs and medications are in some way related to, or used in the treatment of Giardiasis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Medical Encyclopedia:
Harvard Health Guide:
Mirtazapin-1A Pharma may be available in the countries listed below.
Mirtazapine is reported as an ingredient of Mirtazapin-1A Pharma in the following countries:
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Definition of Proctitis: An inflammation of the rectum causing discomfort, bleeding, and occasionally, a discharge of mucus or pus.
The following drugs and medications are in some way related to, or used in the treatment of Proctitis. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.
Medical Encyclopedia:
Propyl-Thyracil may be available in the countries listed below.
Propylthiouracil is reported as an ingredient of Propyl-Thyracil in the following countries:
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Hoesmin may be available in the countries listed below.
Benzalkonium chloride (a derivative of Benzalkonium) is reported as an ingredient of Hoesmin in the following countries:
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Indapress may be available in the countries listed below.
Indapamide is reported as an ingredient of Indapress in the following countries:
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Dropia may be available in the countries listed below.
Pioglitazone hydrochloride (a derivative of Pioglitazone) is reported as an ingredient of Dropia in the following countries:
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Lansoprazol Orifarm may be available in the countries listed below.
Lansoprazole is reported as an ingredient of Lansoprazol Orifarm in the following countries:
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Treating certain worm infections (eg, pinworm, roundworm).
Reese's Pinworm Medicine is an anthelmintic agent. It works by paralyzing the nervous system of intestinal parasites (worms). The parasite is then passed in the stool.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Reese's Pinworm Medicine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Reese's Pinworm Medicine. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Reese's Pinworm Medicine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Reese's Pinworm Medicine as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Reese's Pinworm Medicine.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Diarrhea; dizziness; drowsiness; headache; loss of appetite; nausea; stomach cramps; trouble sleeping; vomiting.
Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Reese's Pinworm Medicine side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Store Reese's Pinworm Medicine at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Reese's Pinworm Medicine out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Reese's Pinworm Medicine. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Treating symptoms associated with a certain bladder problem (interstitial cystitis). It may also be used for other conditions as determined by your doctor.
Dimethyl Sulfoxide is a sterile solution of dimethyl sulfoxide. It is unknown exactly how Dimethyl Sulfoxide works.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Dimethyl Sulfoxide. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Dimethyl Sulfoxide. However, no specific interactions with Dimethyl Sulfoxide are known at this time.
This may not be a complete list of all interactions that may occur. Ask your health care provider if Dimethyl Sulfoxide may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Dimethyl Sulfoxide as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Dimethyl Sulfoxide.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Bladder discomfort; garlic odor on breath or skin for up to 72 hours; garlic taste for several hours.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); eye pain or burning; vision changes.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
See also: Dimethyl Sulfoxide side effects (in more detail)
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately.
Store Dimethyl Sulfoxide at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Protect from light. Do not store in the bathroom. Keep Dimethyl Sulfoxide out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Dimethyl Sulfoxide. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Clarus may be available in the countries listed below.
Isotretinoin is reported as an ingredient of Clarus in the following countries:
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Ridinox may be available in the countries listed below.
Idoxuridine is reported as an ingredient of Ridinox in the following countries:
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Class: Vitamin B Complex
ATC Class: A11HA04
VA Class: VT106
CAS Number: 83-88-5
Water-soluble, B complex vitamin.a b
Used to prevent and treat riboflavin deficiency (ariboflavinosis).a b
Riboflavin deficiency may occur in patients with long-standing infections, liver disease, alcoholism, malignancy, cardiac disease, diabetes mellitus, and those taking probenecid.a
Adequate intake needed to prevent riboflavin deficiency (ariboflavinosis).101 b
Adequate intake of riboflavin usually can be accomplished through consumption of foodstuffs, including milk, bread products, and fortified cereals.101 b
Estimated Average Requirement (EAR) and Recommended Dietary Allowance (RDA) in adults based on a combination of criteria including erythrocyte glutathione reductase activity and urinary excretion of riboflavin.101 b
Adequate intake (AI) established for infants ≤6 months of age based on riboflavin intake of infants fed principally human milk;b AI for infants 7–12 months of age based on the AI for younger infants and data from adults.b
EAR and RDA for children 1–18 years of age based on data in adults.101 b
Used as a urine marker when mixed with various drugs to test for patient compliance with the therapeutic regimen of these drugs.a
Has been used for prophylaxis of migraine headache† to decrease the frequency and duration of attacks.102
Correct poor dietary habits and consider a multivitamin preparation containing riboflavin in patients with vitamin deficiencies since poor dietary habits often result in concurrent deficiencies.a
Administer orally.a e
May be given by IM injection or IV infusion as a component of a multivitamin injection.a A parenteral formulation containing riboflavin alone is not currently commercially available.a
Administer orally, preferably with food.e
Usually, 3–10 mg daily.a
Infants <6 months of age: AI is 0.3 mg (0.04 mg/kg) daily.101
Infants 6–12 months of age: AI is 0.4 mg (0.04 mg/kg) daily.101
Children 1–3 years of age: RDA is 0.5 mg daily.101
Children 4–8 years of age: RDA is 0.6 mg daily.101
Children 9–13 years of age: RDA is 0.9 mg daily.101
Girls 14–19 years of age: RDA is 1 mg daily.101
Boys 14–19 years of age: RDA is 1.3 mg daily.101
Usually, 5–30 mg daily given in divided doses.a
Patients with normocytic, normochromic anemia: 10 mg daily usually increases reticulocyte count within a few days.a
Women ≥19 years of age: RDA is 1.1 mg daily.101
Men ≥19 years of age: RDA is 1.3 mg daily.101
These RDAs will not meet the needs of individuals with severe malabsorption.101 b
400 mg daily; maximal benefit may occur after 3 months of prophylaxis therapy.102
Pregnant women: RDA is 1.4 mg daily.101 Riboflavin intake exceeding this RDA may be needed by women who are pregnant with more than one fetus.101 b
Lactating women: RDA is 1.6 mg daily.101 Riboflavin intake exceeding this RDA may be needed by mothers nursing more than one infant.101 b
May require additional riboflavin intake in patients who are extremely physically active.b
Patients undergoing hemodialysis or peritoneal dialysis may require additional riboflavin.b
Known hypersensitivity to riboflavin or any ingredient in the formulation.c
Increased riboflavin deficiency risk in patients with cancer, cardiac disease, or diabetes mellitus.b
Consider the cautions, precautions, and contraindications associated with other drug(s) and vitamins in fixed-combination preparations.c
Category A.d Category C (for dosages >RDA).d (See Special Populations under Dosage and Administration.)
Distributed into human milk.101 a d
Usually nontoxic even in large doses.a b
Drug or Test | Interaction | Comments |
|---|---|---|
Aminoglyosides (kanamycin, streptomycin) | Possible decreased antibiotic activity c | |
Bleomycin | Inactivated in vitro by riboflavinc | |
Erythromycin | Possible decreased antibiotic activity c | |
Probenecid | Decreased absorption of riboflavina | |
Propantheline | Propantheline may delay the rate of riboflavin absorption, but increase the total amount absorbed a | |
Spectrometry or color reaction urinalysis | Possible color interferencea | |
Tests for catecholamines | Possible false elevations in fluorometric determinations of plasma or urinary catecholaminesa | |
Tests for urobilinogen | Possible false elevations in fluorometric determinations of plasma or urinary urobilinogena |
Readily absorbed from the upper GI tract.a b Rate of absorption is proportional to intake.b
Therapeutic response in riboflavin-deficient patients may require several days for ocular and dermatologic manifestations of deficiency to improve.a
Following oral administration in deficient patients with normocytic, normochromic anemia, an increase in reticulocyte count usually occurs within a few days.a
Food increases extent of absorption.a b
Extent of absorption is decreased in patients with hepatitis, cirrhosis, or biliary obstruction.a
Widely distributed into most tissues, including GI mucosal cells, erythrocytes, and the liver as riboflavin 5-phosphate (flavin mononucleotide [FMN]) and flavin adenine dinucleotide (FAD).a b Free riboflavin is present in the retina.a
Stored in limited amounts in the liver, spleen, kidneys, and heart, mainly as FAD.a
Crosses the placenta and is distributed into milk.101
About 60% as FAD and FMN.a
Phosphorylated to FMN in GI mucosal cells, erythrocytes, and the liver; FMN is converted to FAD in the liver.a
Urine (about 9%) as unchanged drug; fate of the remainder of the dose not determined.a
Following oral or IM administration, about 66–84 minutes.a
Removal by hemodialysis is slower than normal renal excretion.a
In neonates, urinary excretion is slow; however, the cumulative amount excreted is similar to the amount excreted by older infants.b
Tight, light-resistant containers at 15–30°C.a
For information on systemic interactions resulting from concomitant use, see Interactions.
Incompatible with alkaline solutions.a
An exogenous source of riboflavin is required for tissue respiration.a
Converts to coenzymes (FMN and FAD) involved in oxidation-reduction reactions of organic substrates and in intermediary metabolism.a b e
Flavocoenzymes are involved in the formation of some vitamins and their coenzymes, including niacin, vitamin B6, and vitamin B12.101 b
Indirectly involved in maintaining erythrocyte integrity.a
Importance of proper dietary habits, including taking appropriate AI or RDA of vitamin B2.
Inform patients that large doses of riboflavin can result in bright yellow urine.a
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.b
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.b
Importance of informing patients of other important precautionary information. (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
Riboflavin, riboflavin 5-phosphate, and riboflavin 5-phosphate sodium are also commercially available in combination with other vitamins, minerals, amino acids, cerebral stimulants, protein supplements, infant formulas, enzymes, hormones, sedatives, laxatives, and unsaturated fatty acids.a For IM injection, riboflavin is commercially available in combination with other vitamins and iron.a For IV infusion, riboflavin is commercially available in combination with other vitamins.a c
* available from one or more manufacturer, distributor, and/or repackager by generic (nonproprietary) name
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
|---|---|---|---|---|
Bulk | Powder* | |||
Oral | Capsules | 100 mg* | ||
Tablets | 25 mg* | |||
50 mg* | ||||
100 mg* | ||||
Sublingual | Tablets | 25 mg (as flavin mononucleotide [coenzymated])* | Riboflavin Sublingual Tablets |
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions August 01, 2009. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
† Use is not currently included in the labeling approved by the US Food and Drug Administration.
Only references cited for selected revisions after 1984 are available electronically.
100. National Research Council Food and Nutrition Board Subcommittee on the Tenth Edition of the RDAs. Recommended dietary allowances. 10th ed. Washington, DC: National Academies Press; 1989:132-7.
101. Standing Committee on the Scientific Evaluation of Dietary Reference Intakes of the Food and Nutrition Board, Institute of Medicine, National Academy of Sciences. Dietary reference intakes for thiamin, riboflavin, niacin, vitamin B6, folate, vitamin B12, pantothenic acid, biotin, and choline. Washington, DC: National Academies Press; 1998.
102. Schoenen J, Jacquy J, Lenaerts M. Effectiveness of high-dose riboflavin in migraine prophylaxis: a randomized controlled trial. Neurology. 1998; 50:466-70. [IDIS 401485] [PubMed 9484373]
a. AHFS Drug Information 2009. McEvoy GK, ed. Riboflavin. Bethesda, MD: American Society of Health-System Pharmacists; 2009.
b. Otten JJ, Hellwig JP, Meyers LD, eds. Dietary reference intakes: the essential guide to nutritional requirements. Washington, DC: National Academies Press; 2006.
c. Baxter. INFUVITE Adult (Multiple vitamins for Infusion) prescribing information. Deerfield, IL; 2004 May.
d. Briggs GG, Freeman RK, Yaffe SJ. Drugs in pregnancy and lactation. 7th ed. Baltimore , MD: Williams & Wilkins; 2005:1410–11.
e. Nature’s Way. Vitamin B2 (riboflavin) capsules product information. Springville, UT; 2004.
Movipride may be available in the countries listed below.
Bromopride is reported as an ingredient of Movipride in the following countries:
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Theophyllin Lindopharm may be available in the countries listed below.
Theophylline is reported as an ingredient of Theophyllin Lindopharm in the following countries:
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Alprazolam Unilan may be available in the countries listed below.
Alprazolam is reported as an ingredient of Alprazolam Unilan in the following countries:
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Nimodipina EG may be available in the countries listed below.
Nimodipine is reported as an ingredient of Nimodipina EG in the following countries:
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Iosan may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Povidone-Iodine is reported as an ingredient of Iosan in the following countries:
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Meligran may be available in the countries listed below.
Buflomedil hydrochloride (a derivative of Buflomedil) is reported as an ingredient of Meligran in the following countries:
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Karbasif may be available in the countries listed below.
Carbamazepine is reported as an ingredient of Karbasif in the following countries:
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Sulpigut may be available in the countries listed below.
Sulpiride is reported as an ingredient of Sulpigut in the following countries:
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Ostiseptil may be available in the countries listed below.
Urea is reported as an ingredient of Ostiseptil in the following countries:
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Tamox may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Tamox in the following countries:
Tamoxifen citrate (a derivative of Tamoxifen) is reported as an ingredient of Tamox in the following countries:
International Drug Name Search
In the US, Stavudine (stavudine systemic) is a member of the drug class nucleoside reverse transcriptase inhibitors (NRTIs) and is used to treat HIV Infection and Nonoccupational Exposure.
US matches:
Prop.INN
J05AF04
0003056-17-5
C10-H12-N2-O4
224
Antiviral agent, HIV reverse transcriptase inhibitor
1-(2,3-Dideoxy-ß-D-glycero-pent-2-enofuranosyl)thymine
International Drug Name Search
Glossary
| BAN | British Approved Name |
| 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 |
Tosuxacin may be available in the countries listed below.
Tosufloxacin tosilate (a derivative of Tosufloxacin) is reported as an ingredient of Tosuxacin in the following countries:
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Tramadol HCl Actavis may be available in the countries listed below.
Tramadol hydrochloride (a derivative of Tramadol) is reported as an ingredient of Tramadol HCl Actavis in the following countries:
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Colifoam may be available in the countries listed below.
UK matches:
Hydrocortisone is reported as an ingredient of Colifoam in the following countries:
Hydrocortisone 21-acetate (a derivative of Hydrocortisone) is reported as an ingredient of Colifoam in the following countries:
International Drug Name Search
Glossary
| SPC | Summary of Product Characteristics (UK) |
RAN-Risperidone may be available in the countries listed below.
Risperidone is reported as an ingredient of RAN-Risperidone in the following countries:
International Drug Name Search
Deroxat may be available in the countries listed below.
Paroxetine is reported as an ingredient of Deroxat in the following countries:
Paroxetine hydrochloride (a derivative of Paroxetine) is reported as an ingredient of Deroxat in the following countries:
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Topilex may be available in the countries listed below.
Topiramate is reported as an ingredient of Topilex in the following countries:
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Magnesium-Diasporal 2mmol/4mmol may be available in the countries listed below.
Magnesium Sulfate heptahydrate (a derivative of Magnesium Sulfate) is reported as an ingredient of Magnesium-Diasporal 2mmol/4mmol in the following countries:
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Treating heartburn or irritation of the esophagus caused by gastroesophageal reflux disease (GERD). It may be used to treat and maintain healing of severe irritation of the esophagus (erosive esophagitis). It may be used for short-term treatment of stomach or small intestinal ulcers. It may be used to maintain healing of stomach or small intestinal ulcers. It may be used to treat conditions that cause your body to make too much stomach acid (eg, Zollinger-Ellison syndrome). It may also be used for other conditions as determined by your doctor.
Ranitidine is an H2-receptor blocker. It works by blocking the action of histamine in the stomach. This reduces the amount of acid the stomach makes. Reducing stomach acid helps to reduce heartburn, heal irritation of the esophagus, and heal ulcers of the stomach or intestines.
Contact your doctor or health care provider right away if any of these apply to you.
Some medical conditions may interact with Ranitidine. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:
Some MEDICINES MAY INTERACT with Ranitidine. Tell your health care provider if you are taking any other medicines, especially any of the following:
This may not be a complete list of all interactions that may occur. Ask your health care provider if Ranitidine may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.
Use Ranitidine as directed by your doctor. Check the label on the medicine for exact dosing instructions.
Ask your health care provider any questions you may have about how to use Ranitidine.
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:
Constipation; diarrhea; headache; nausea; stomach upset.
Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue; unusual hoarseness); change in the amount of urine produced; confusion; dark urine; depression; fast, slow, or irregular heartbeat; fever, chills, or sore throat; hallucinations; severe or persistent headache or stomach pain; unusual bruising or bleeding; yellowing of the eyes or skin.
This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.
Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include dizziness; trouble walking.
Store Ranitidine at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Ranitidine out of the reach of children and away from pets.
This information is a summary only. It does not contain all information about Ranitidine. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.
Bicalutamide Medac may be available in the countries listed below.
Bicalutamide is reported as an ingredient of Bicalutamide Medac in the following countries:
International Drug Name Search
In the US, Pamabrom (pamabrom systemic) is a member of the drug class miscellaneous diuretics and is used to treat Abdominal Distension, Edema and Premenstrual Dysphoric Disorder.
US matches:
USAN
0000606-04-2
C11-H18-Br-N5-O3
348
Diuretic agent
1H-Purine-2,6-dione, 8-bromo-3,7-dihydro-1,3-dimethyl-, compd. with 2-amino-2-methyl-1-propanol (1:1)
International Drug Name Search
Glossary
| IS | Inofficial Synonym |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| USAN | United States Adopted Name |
Cefozim may be available in the countries listed below.
Ceftazidime is reported as an ingredient of Cefozim in the following countries:
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Ranclic may be available in the countries listed below.
Pirenzepine dihydrochloride (a derivative of Pirenzepine) is reported as an ingredient of Ranclic in the following countries:
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Tensiol may be available in the countries listed below.
Olmesartan Medoxomil is reported as an ingredient of Tensiol in the following countries:
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Ceftazidime Panpharma may be available in the countries listed below.
Ceftazidime pentahydrate (a derivative of Ceftazidime) is reported as an ingredient of Ceftazidime Panpharma in the following countries:
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Diart may be available in the countries listed below.
Azosemide is reported as an ingredient of Diart in the following countries:
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Platinex may be available in the countries listed below.
Cisplatin is reported as an ingredient of Platinex in the following countries:
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Fluoxetina Bexal may be available in the countries listed below.
Fluoxetine hydrochloride (a derivative of Fluoxetine) is reported as an ingredient of Fluoxetina Bexal in the following countries:
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Tenasil may be available in the countries listed below.
Terbinafine hydrochloride (a derivative of Terbinafine) is reported as an ingredient of Tenasil in the following countries:
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Lanzogastro may be available in the countries listed below.
Lansoprazole is reported as an ingredient of Lanzogastro in the following countries:
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Theotard may be available in the countries listed below.
Theophylline is reported as an ingredient of Theotard in the following countries:
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Arthri Dog may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Phenylbutazone calcium salt (a derivative of Phenylbutazone) is reported as an ingredient of Arthri Dog in the following countries:
Prednisolone 21-acetate (a derivative of Prednisolone) is reported as an ingredient of Arthri Dog in the following countries:
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Paralen may be available in the countries listed below.
Paracetamol is reported as an ingredient of Paralen in the following countries:
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In the US, MetroGel (metronidazole topical) is a member of the drug class topical acne agents and is used to treat Perioral Dermatitis and Rosacea.
US matches:
UK matches:
Metronidazole is reported as an ingredient of MetroGel in the following countries:
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Glossary
| SPC | Summary of Product Characteristics (UK) |
