Etilmorfina may be available in the countries listed below.
Etilmorfina (DCIT) is also known as Ethylmorphine (BAN)
International Drug Name Search
Glossary
| BAN | British Approved Name |
| DCIT | Denominazione Comune Italiana |
Malgacid may be available in the countries listed below.
Hydrotalcite is reported as an ingredient of Malgacid in the following countries:
International Drug Name Search
Clotrimazolo may be available in the countries listed below.
Clotrimazolo (DCIT) is known as Clotrimazole in the US.
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Glossary
| DCIT | Denominazione Comune Italiana |
Felodipine Hexal may be available in the countries listed below.
Felodipine is reported as an ingredient of Felodipine Hexal in the following countries:
International Drug Name Search
Lincomycine VMD may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Lincomycin hydrochloride monohydrate (a derivative of Lincomycin) is reported as an ingredient of Lincomycine VMD in the following countries:
International Drug Name Search
Iodio Farve may be available in the countries listed below.
Iodine is reported as an ingredient of Iodio Farve in the following countries:
Potassium Iodide is reported as an ingredient of Iodio Farve in the following countries:
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E-bac may be available in the countries listed below.
Erythromycin is reported as an ingredient of E-bac in the following countries:
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Amos Anti Melkziektestoot may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Colecalciferol is reported as an ingredient of Amos Anti Melkziektestoot in the following countries:
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Rec.INN
B01AC10
0063610-08-2
C18-H17-N-O3
295
Antiplatelet agent, reversible cyclooxygenase inhibitor
Benzeneacetic acid, 4-(1,3-dihydro-1-oxo-2H-isoindol-2-yl)-α-ethyl-, (±)-
International Drug Name Search
Glossary
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
In some countries, this medicine may only be approved for veterinary use.
In the US, Etodolac (etodolac systemic) is a member of the drug class nonsteroidal anti-inflammatory agents and is used to treat Juvenile Rheumatoid Arthritis, Osteoarthritis, Pain and Rheumatoid Arthritis.
US matches:
Rec.INN
M01AB08
0041340-25-4
C17-H21-N-O3
287
Analgesic, antipyretic and anti-inflammatory agent
Non-steroidal anti-inflammatory drug, NSAID
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-
International Drug Name Search
Glossary
| BAN | British Approved Name |
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Ciprofloxacine Actavis may be available in the countries listed below.
Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Ciprofloxacine Actavis in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
Rec.INN
0147116-67-4
C32-H40-N2-O
468
Antiemetic
(2S,3S)-N-(5-tert-butyl-2-methoxybenzyl)-2-(diphenylmethyl)-1-azabicyclo[2.2.2]octan-3-amine (WHO)
(2S,3S)-N-[5-(1,1-Dimethylethyl)-2-methoxybenzyl]-2-(diphenylmethyl)-1-azabicyclo-[2.2.2]octan-3-amin (IUPAC)
International Drug Name Search
Glossary
| IUPAC | International Union of Pure and Applied Chemistry |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| WHO | World Health Organization |
Xilinã may be available in the countries listed below.
Lidocaine hydrochloride (a derivative of Lidocaine) is reported as an ingredient of Xilinã in the following countries:
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Murhinal may be available in the countries listed below.
Carbocisteine is reported as an ingredient of Murhinal in the following countries:
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Polysporin Itch Relief may be available in the countries listed below.
Pramocaine hydrochloride (a derivative of Pramocaine) is reported as an ingredient of Polysporin Itch Relief in the following countries:
Zinc Acetate is reported as an ingredient of Polysporin Itch Relief in the following countries:
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Amoxicilline Disphar may be available in the countries listed below.
Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Amoxicilline Disphar in the following countries:
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GEL-PHAN may be available in the countries listed below.
Gelatin is reported as an ingredient of GEL-PHAN in the following countries:
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Makrosilin may be available in the countries listed below.
Ampicillin trihydrate (a derivative of Ampicillin) is reported as an ingredient of Makrosilin in the following countries:
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Itranol may be available in the countries listed below.
Itraconazole is reported as an ingredient of Itranol in the following countries:
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Bupivacaina Fisiopharma may be available in the countries listed below.
Bupivacaine hydrochloride (a derivative of Bupivacaine) is reported as an ingredient of Bupivacaina Fisiopharma in the following countries:
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BetaSalbe KSK may be available in the countries listed below.
Betamethasone 17α-valerate (a derivative of Betamethasone) is reported as an ingredient of BetaSalbe KSK in the following countries:
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Pseudoéphédrine may be available in the countries listed below.
Pseudoéphédrine (DCF) is known as Pseudoephedrine in the US.
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Glossary
| DCF | Dénomination Commune Française |
Toliken may be available in the countries listed below.
Clindamycin is reported as an ingredient of Toliken in the following countries:
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Rec.INN
C04AX11
0002179-37-5
C19-H31-N-O
289
Vasodilator, peripheric
1-Propanamine, N,N-dimethyl-3-[[1-(phenylmethyl)cycloheptyl]oxy]-
International Drug Name Search
Glossary
| DCF | Dénomination Commune Française |
| DCIT | Denominazione Comune Italiana |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Amoxy Active 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 Amoxy Active in the following countries:
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Hipermex may be available in the countries listed below.
Meclozine dihydrochloride (a derivative of Meclozine) is reported as an ingredient of Hipermex in the following countries:
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Monocorat may be available in the countries listed below.
Isosorbide Mononitrate is reported as an ingredient of Monocorat in the following countries:
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Brot may be available in the countries listed below.
Metformin hydrochloride (a derivative of Metformin) is reported as an ingredient of Brot in the following countries:
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Kenalog Intra-articular / Intramuscular Injection
Kenalog Intra-articular / Intramuscular Injection contains triamcinolone acetonide 40mg per ml of sterile suspension.
Sterile aqueous suspension for injection.
Intra-articular use: for alleviating the joint pain, swelling and stiffness associated with rheumatoid arthritis and osteoarthrosis, with an inflammatory component; also for bursitis, epicondylitis, and tenosynovitis.
Intramuscular use: Where sustained systemic corticosteroid treatment is required: Allergic states, e.g. bronchial asthma, seasonal or perennial allergic rhinitis. In seasonal allergies, patients who do not respond to conventional therapy may achieve a remission of symptoms over the entire period with a single intramuscular injection (see Dosage); Endocrine disorders, e.g. primary or secondary adrenocortical insufficiency. Collagen disorders, e.g. during an exacerbation of maintenance therapy of selected cases of SLE or acute rheumatic carditis; Dermatological diseases, e.g. pemphigus, severe dermatitis and Stevens Johnson Syndrome; Rheumatic, Gastrointestinal or Respiratory disorders - as an adjunctive, short-term therapy; Haematological disorders, e.g. acquired (autoimmune) haemolytic anaemia; Neoplastic diseases, e.g. palliative management of leukaemia and lymphomas; Renal disease, such as acute interstitial nephritis, minimal change nephrotic syndrome or lupus nephritis.
Kenalog is for Intra-articular/Intramuscular injection. The safety and efficacy of administration by other routes has yet to be established. Strict aseptic precautions should be observed. Since the duration of effect is variable, subsequent doses should be given when symptoms recur and not at set intervals.
Intra-Articular Injection: For intra-articular administration or injection into tendon sheaths and bursae, the dose of Kenalog Injection may vary from 5mg to 10mg (0.125 - 0.25ml) for smaller joints and up to 40mg (1.0ml) for larger joints, depending on the specific disease entity being treated. Single injections into several sites for multiple joint involvement, up to a total of 80mg, have been given without undue reactions.
It is recommended that, when injections are given into the sheaths of short tendons, Adcortyl Injection (triamcinolone acetonide 10mg/ml) should be used. (See under Precautions, re Achilles tendon).
Intramuscular Injection: To avoid the danger of subcutaneous fat atrophy, it is important to ensure that deep intramuscular injection is given into the gluteal site. The deltoid should not be used. Alternate sides should be used for subsequent injections.
Adults and Children over 12 Years: The suggested initial dose is 40mg (1.0ml) injected deeply into the upper, outer quadrant of the gluteal muscle. Subsequent dosage depends on the patient's response and period of relief. Patients with hay fever or pollen asthma who do not respond to conventional therapy may obtain a remission of symptoms lasting throughout the pollen season after a single dose of 40-100mg given when allergic symptoms appear. (See Warnings and Precautions.)
Elderly: Treatment of elderly patients, particularly if long term, should be planned bearing in mind the more serious consequences of the common side effects of corticosteroids in old age, especially osteoporosis, diabetes, hypertension, susceptibility to infection and thinning of the skin. Close clinical supervision is required to avoid life-threatening reactions.
Children from 6-12 Years of Age: The suggested initial dose of 40mg (1.0ml injected deeply into the gluteal muscle should be scaled according to the severity of symptoms and the age and weight of the child. Kenalog is not recommended for children under six years. Growth and development of children on prolonged corticosteroid therapy should be carefully observed. (See Warnings and Precautions.)
Triamcinolone withdrawal: In patients who have received more than physiological doses of Kenalog (more than one injection during a three week period), withdrawal should not be abrupt. The dose should be reduced and the dosage interval increased until a dose of not more than 40mg and a dosage interval of at least three weeks have been achieved as the dose of systemic corticosteroid is reduced. Clinical assessment of disease activity may be needed.
Abrupt withdrawal of short term systemic corticosteroid treatment is appropriate if it is considered that the disease is unlikely to relapse. A single dose, which is not repeated within a three week period, is unlikely to lead to clinically relevant hpa-axis suppression in the majority of patients. However, in the following patient groups, gradual withdrawal of systemic corticosteroid therapy should always be considered:
|
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Hypersensitivity to any of the ingredients.
Systemic infections unless specific anti-infective therapy is employed.
Administration by intravenous or intrathecal injection.
Warnings
(Intra-Articular Injection):
Patients should be specifically warned to avoid over-use of joints in which symptomatic benefit has been obtained. Severe joint destruction with necrosis of bone may occur if repeated intra-articular injections are given over a long period of time. Care should be taken if injections are given into tendon sheaths to avoid injection into the tendon itself.
Due to the absence of a true tendon sheath, the Achilles tendon should not be injected with depot corticosteroids.
(Intramuscular Injection):
During prolonged therapy a liberal protein intake is essential to counteract the tendency to gradual weight loss sometimes associated with negative nitrogen balance and wasting of skeletal muscle.
Precautions:
Intra-articular injection should not be carried out in the presence of active infection in or near joints. The preparation should not be used to alleviate joint pain arising from infectious states such as gonococcal or tubercular arthritis.
Undesirable effects may be minimised using the lowest effective dose for the minimum period, and by administering the daily requirement, whenever possible, as a single morning dose on alternate days. Frequent patient review is required to titrate the dose appropriately against disease activity. (See dosage section).
Adrenal cortical atrophy develops during prolonged therapy and may persist for years after stopping treatment. Withdrawal of corticosteroids after prolonged therapy must, therefore, always be gradual to avoid acute adrenal insufficiency and should be tapered off over weeks or months according to the dose and duration of treatment. During prolonged therapy any intercurrent illness, trauma or surgical procedure will require a temporary increase in dosage. If corticosteroids have been stopped following prolonged therapy they may need to be reintroduced temporarily.
Patients should carry steroid treatment cards which give clear guidance on the precautions to be taken to minimise risk and which provide details of prescriber, drug, dosage and the duration of treatment.
Suppression of the inflammatory response and immune function increases the susceptibility to infections and their severity. The clinical presentation may often be atypical and serious infections such as septicaemia and tuberculosis may be masked and may reach an advanced stage before being recognised.
Chickenpox is of particular concern since this normally minor illness may be fatal in immunosuppressed patients. Patients (or parents of children receiving Kenalog Injection) without a definite history of chickenpox should be advised to avoid close personal contact with chickenpox or herpes zoster. If exposed they should seek urgent medical attention. Passive immunisation with varicella zoster immunoglobulin (VZIG) is needed by exposed non- immune patients who are receiving systemic corticosteroids or who have used them within the previous 3 months; this should be given within 10 days of exposure to chickenpox. If a diagnosis of chickenpox is confirmed, the illness warrants specialist care and urgent treatment. Corticosteroids should not be stopped and the dose may need to be increased.
During corticosteroid therapy antibody response will be reduced and therefore affect the patient's response to vaccines. Live vaccines should not be administered.
Special Precautions:
Particular care is required when considering use of systemic corticosteroids in patients with the following conditions and frequent patient monitoring is necessary.
Recent intestinal anastomoses, diverticulitis, thrombophlebitis, existing or previous history of severe affective disorders (especially previous steroid psychosis), exanthematous disease, chronic nephritis, or renal insufficiency, metastatic carcinoma, osteoporosis (post-menopausal females are particularly at risk); in patients with an active peptic ulcer (or a history of peptic ulcer). Myasthenia gravis. Latent or healed tuberculosis; in the presence of local or systemic viral infection, systemic fungal infections or in active infections not controlled by antibiotics. In acute psychoses; in acute glomerulonephritis. Hypertension; congestive heart failure; glaucoma (or a family history of glaucoma), previous steroid myopathy or epilepsy. Liver failure.
Corticosteroid effects may be enhanced in patients with hypothyroidism or cirrhosis.
Diabetes may be aggravated, necessitating a higher insulin dosage. Latent diabetes mellitus may be precipitated.
Menstrual irregularities may occur, and this possibility should be mentioned to female patients.
Rare instances of anaphylactoid reactions have occurred in patients receiving corticosteroids, especially when a patient has a history of drug allergies.
All corticosteroids increase calcium excretion.
Aspirin should be used cautiously in conjunction with corticosteroids in patients with hypoprothrombinaemia.
Use in Children:
Kenalog is not recommended for children under six years. Corticosteroids cause dose-related growth retardation in infancy, childhood and adolescence which may be irreversible, therefore growth and development of children on prolonged corticosteroid therapy should be carefully observed.
Use in Elderly:
The common adverse effects of systemic corticosteroids may be associated with more serious consequences in old age, especially osteoporosis, hypertension, hypokalaemia, diabetes, susceptibility to infection and thinning of the skin. Close clinical supervision is required to avoid life-threatening reactions.
Barbiturates, phenytoin, rifampicin, rifabutin, carbamazepine, primidone and aminoglutethimide may enhance the metabolic clearance of corticosteroids, resulting in decreased therapeutic effects.
Corticosteroids antagonise the effects of hypoglycaemic agents (including insulin), anti-hypertensives and diuretics. The hypokalaemic effects of acetazolamide, loop diuretics, thiazide diuretics and carbenoxolone are enhanced.
The efficacy of coumarin anticoagulants may be enhanced by concurrent corticosteroid therapy and close monitoring of the INR or prothrombin time is required to avoid spontaneous bleeding.
The renal clearance of salicylates is increased by corticosteroids and steroid withdrawal may result in salicylate intoxication.
The ability of corticosteroids to cross the placenta varies between individual drugs, however triamcinolone does cross the placenta.
Administration of corticosteroids to pregnant animals can cause abnormalities of foetal development including cleft palate, intra-uterine growth retardation and effects on brain growth and development. There is no evidence that corticosteroids result in an increased incidence of congenital abnormalities, such as cleft palate / lip in man. However, when administered for prolonged periods or repeatedly during pregnancy, corticosteroids may increase the risk of intra-uterine growth retardation. Hypoadrenalism may, in theory, occur in the neonate following prenatal exposure to corticosteroids but usually resolves spontaneously following birth and is rarely clinically important. As with all drugs, corticosteroids should only be prescribed when the benefits to the mother and child outweigh the risks. When corticosteroids are essential, however, patients with normal pregnancies may be treated as though they were in the non-gravid state.
Lactation:
Corticosteroids may pass into breast milk, although no data are available for triamcinolone. Infants of mothers taking high doses of systemic corticosteroids for prolonged periods may have a degree of adrenal suppression.
None known.
Where adverse reactions occur they are usually reversible on cessation of therapy. The incidence of predictable side-effects, including hypothalamic-pituitary-adrenal suppression correlate with the relative potency of the drug, dosage, timing of administration and duration of treatment. (See Warnings and Precautions).
Absorption of triamcinolone following injection by the intra-articular route is rare. However, patients should be watched closely for the following adverse reactions which may be associated with any corticosteroid therapy:
Anti-inflammatory and immunosuppressive effects: Increased susceptibility and severity of infections with suppression of clinical symptoms and signs, opportunistic infections, recurrence of dormant tuberculosis. (See Warnings and Precautions).
Fluid and electrolyte disturbances: Sodium retention, fluid retention, congestive heart failure in susceptible patients, potassium loss, cardiac arrhythmias or ECG changes due to potassium deficiency, hypokalaemic alkalosis, increased calcium excretion and hypertension.
Musculoskeletal: Muscle weakness, fatigue, steroid myopathy, loss of muscle mass, osteoporosis, avascular osteonecrosis, vertebral compression fractures, delayed healing of fractures, aseptic necrosis of femoral and humeral heads, pathological fractures of long bones and spontaneous fractures, tendon rupture.
Gastrointestinal: Dyspepsia, peptic ulcer with possible subsequent perforation and haemorrhage, pancreatitis, abdominal distension and ulcerative oesophagitis, candidiasis.
Dermatological: Impaired wound healing, thin fragile skin, petechiae and ecchymoses, facial erythema, increased sweating, purpura, striae, hirsutism, acneiform eruptions, lupus erythematous-like lesions and suppressed reactions to skin tests.
Neurological: Euphoria, psychological dependence, depression, insomnia, convulsions, increased intracranial pressure with papilloedema (pseudo-tumour cerebri) usually after treatment, vertigo, headache, neuritis or paraesthesias and aggravation of pre
Endocrine: Menstrual irregularities and amenorrhoea; development of the Cushingoid state; suppression of growth in childhood and adolescence; secondary adrenocortical and pituitary unresponsiveness, particularly in times of stress (e.g. trauma, surgery or illness); decreased carbohydrate tolerance; manifestations of latent diabetes mellitus and increased requirements for insulin or oral hypoglycaemic agents in diabetes, weight gain. Negative protein and calcium balance. Increased appetite.
Ophthalmic: Posterior supcapsular cataracts, increased intraocular pressure, glaucoma, exophthalmos, papilloedema, corneal or scleral thinning, exacerbation of ophthalmic viral or fungal diseases.
Others: Necrotising angiitis, thrombophlebitis, thromboembolism, leucocytosis, insomnia, syncopal episodes and anaphylactoid reactions, particularly where there is a history of drug allergies.
Withdrawal Symptoms and Signs:
On withdrawal, fever, myalgia, arthralgia, rhinitis, conjunctivitis, painful itchy skin nodules and weight loss may occur. Too rapid a reduction in dose following prolonged treatment can lead to acute adrenal insufficiency, hypotension and death. (See Warnings and Precautions.)
Intra-Articular Injection:
Reactions following intra-articular administration have been rare. In a few instances, transient flushing and dizziness have occurred. Pain and other local symptoms may continue for a short time before effective relief is obtained, but an increase in joint discomfort has seldom occurred. Local fat atrophy may occur if the injection is not given into the joint space, but is temporary and disappears within a few weeks to months.
Not applicable.
Triamcinolone acetonide is a synthetic glucocorticoid with marked anti-inflammatory and anti-allergic actions.
Intra-Articular Injection: Following local injection, relief of pain and swelling and greater freedom of movement are usually obtained within a few hours.
Intramuscular Injection: Provides an extended duration of therapeutic effect and fewer side effects of the kind associated with oral corticosteroid therapy, particularly gastro-intestinal reactions such as peptic ulceration. Studies indicate that, following a single intramuscular dose of 80mg triamcinolone acetonide, adrenal suppression occurs within 24 - 48 hours and then gradually returns to normal, usually in approximately three weeks. This finding correlates closely with the extended duration of therapeutic action of triamcinolone acetonide.
Triamcinolone acetonide may be absorbed into the systemic circulation from synovial spaces. However clinically significant systemic levels after intra-articular injection are unlikely to occur except perhaps following treatment of large joints with high doses. Systemic effects do not ordinarily occur with intra-articular injections when the proper techniques of administration and the recommended dosage regimens are observed.
Triamcinolone acetonide is absorbed slowly, though almost completely, following depot administration by deep intramuscular injection; biologically active levels are achieved systemically for prolonged periods (weeks to months). In common with other corticosteroids, triamcinolone is metabolised largely hepatically but also by the kidney and is excreted in urine. The main metabolic route is 6-beta-hydroxylation; no significant hydrolytic cleavage of the acetonide occurs.
In view of the hepatic metabolism and renal excretion of triamcinolone acetonide, functional impairments of the liver or kidney may affect the pharmacokinetics of the drug.
See 4.6 Pregnancy and Lactation.
Benzyl alcohol, polysorbate 80, sodium carboxymethylcellulose, sodium chloride, water.
The injection should not be physically mixed with other medicinal products.
36 months
In an upright position below 25°C: avoid freezing.
Carton containing 5 x 1ml glass vials or individually cartoned 1ml and 2ml syringes.
No special handling instructions.
E.R. Squibb & Sons Ltd.
BMS House
141-149 Staines Road
Hounslow
Middlesex TW3 3JA
PL 0034/5045R
July 1986
March 1999
Maxalac may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Cefuroxime sodium salt (a derivative of Cefuroxime) is reported as an ingredient of Maxalac in the following countries:
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Tazko may be available in the countries listed below.
Felodipine is reported as an ingredient of Tazko in the following countries:
Ramipril is reported as an ingredient of Tazko in the following countries:
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Pantin-D may be available in the countries listed below.
Domperidone is reported as an ingredient of Pantin-D in the following countries:
Pantoprazole is reported as an ingredient of Pantin-D in the following countries:
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Fluorouracil-Faulding may be available in the countries listed below.
Fluorouracil is reported as an ingredient of Fluorouracil-Faulding in the following countries:
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Monoket retard may be available in the countries listed below.
Isosorbide Mononitrate is reported as an ingredient of Monoket retard in the following countries:
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Rispimed may be available in the countries listed below.
Risperidone is reported as an ingredient of Rispimed in the following countries:
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Taimac may be available in the countries listed below.
Magaldrate is reported as an ingredient of Taimac in the following countries:
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In the US, Fluvastatin (fluvastatin systemic) is a member of the drug class statins and is used to treat High Cholesterol, High Cholesterol - Familial Heterozygous, Hyperlipoproteinemia, Hyperlipoproteinemia Type IIa - Elevated LDL and Hyperlipoproteinemia Type IIb - Elevated LDL VLDL.
US matches:
UK matches:
Rec.INN
C10AA04
0093957-54-1
C24-H26-F-N-O4
411
Antilipemic agent, HMG CoA reductase inhibitor (statin)
(±)-(3R*,5S*,6E)-7-[3-(p-Fluorophenyl)-1-isopropylindol-2-yl]-3,5-dihydroxy-6-heptenoic acid
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Glossary
| BAN | British Approved Name |
| BANM | British Approved Name (Modified) |
| DCF | Dénomination Commune Française |
| IS | Inofficial Synonym |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| SPC | Summary of Product Characteristics (UK) |
| USAN | United States Adopted Name |
Clint may be available in the countries listed below.
Allopurinol is reported as an ingredient of Clint in the following countries:
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Ixor may be available in the countries listed below.
Roxithromycin is reported as an ingredient of Ixor in the following countries:
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Lisinopril/Hydrochlorthiazid Sandoz may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Lisinopril/Hydrochlorthiazid Sandoz in the following countries:
Lisinopril dihydrate (a derivative of Lisinopril) is reported as an ingredient of Lisinopril/Hydrochlorthiazid Sandoz in the following countries:
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AP-Loratadine may be available in the countries listed below.
Loratadine is reported as an ingredient of AP-Loratadine in the following countries:
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Alcacyl may be available in the countries listed below.
Acetylsalicylic Acid lysine (a derivative of Acetylsalicylic Acid) is reported as an ingredient of Alcacyl in the following countries:
Carbasalate Calcium is reported as an ingredient of Alcacyl in the following countries:
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Acido pipemidico may be available in the countries listed below.
Acido pipemidico (DCIT) is also known as Pipemidic Acid (Rec.INN)
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Glossary
| DCIT | Denominazione Comune Italiana |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Rec.INN
0000642-83-1
C10-H10-O8
258
Enzyme inhibitor, ß-glucuronidase
D-Glucaric acid, di-þ-lactone, 2,5-diacetate
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Glossary
| IS | Inofficial Synonym |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Razoxane Tecnofarma may be available in the countries listed below.
Dexrazoxane is reported as an ingredient of Razoxane Tecnofarma in the following countries:
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Inflaforte may be available in the countries listed below.
Diclofenac sodium salt (a derivative of Diclofenac) is reported as an ingredient of Inflaforte in the following countries:
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Clopidogrel Sulphate may be available in the countries listed below.
Clopidogrel Sulphate (BANM) is known as Clopidogrel in the US.
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Glossary
| BANM | British Approved Name (Modified) |
Losartan Teva may be available in the countries listed below.
Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Losartan Teva in the following countries:
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Cabergolin AL may be available in the countries listed below.
Cabergoline is reported as an ingredient of Cabergolin AL in the following countries:
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Lebersdan may be available in the countries listed below.
Protoporphyrin Disodium is reported as an ingredient of Lebersdan in the following countries:
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Pecusanol may be available in the countries listed below.
In some countries, this medicine may only be approved for veterinary use.
Dichlorvos is reported as an ingredient of Pecusanol in the following countries:
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Ramipril-AC may be available in the countries listed below.
Ramipril is reported as an ingredient of Ramipril-AC in the following countries:
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Inda-Puren may be available in the countries listed below.
Indapamide hemihydrate (a derivative of Indapamide) is reported as an ingredient of Inda-Puren in the following countries:
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Amlate may be available in the countries listed below.
Amlodipine maleate (a derivative of Amlodipine) is reported as an ingredient of Amlate in the following countries:
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Penicilina Procainica may be available in the countries listed below.
Benzylpenicillin procaine (a derivative of Benzylpenicillin) is reported as an ingredient of Penicilina Procainica in the following countries:
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Coversyl Novum may be available in the countries listed below.
Perindopril arginine (a derivative of Perindopril) is reported as an ingredient of Coversyl Novum in the following countries:
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Citoles may be available in the countries listed below.
Escitalopram is reported as an ingredient of Citoles in the following countries:
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Bascul Balsamico may be available in the countries listed below.
Guaifenesin is reported as an ingredient of Bascul Balsamico in the following countries:
Sulfamethoxazole is reported as an ingredient of Bascul Balsamico in the following countries:
Trimethoprim is reported as an ingredient of Bascul Balsamico in the following countries:
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Cadaprim-R may be available in the countries listed below.
Sulfamethoxazole is reported as an ingredient of Cadaprim-R in the following countries:
Trimethoprim is reported as an ingredient of Cadaprim-R in the following countries:
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Chondroitin Polysulfate is reported as an ingredient of Glucosamine HCl and Chondroitin in the following countries:
Glucosamine hydrochloride (a derivative of Glucosamine) is reported as an ingredient of Glucosamine HCl and Chondroitin in the following countries:
International Drug Name Search
Co-Lisinopril-Ratiopharm may be available in the countries listed below.
Hydrochlorothiazide is reported as an ingredient of Co-Lisinopril-Ratiopharm in the following countries:
Lisinopril is reported as an ingredient of Co-Lisinopril-Ratiopharm in the following countries:
International Drug Name Search
Rec.INN
C04AA31
0003703-79-5
C12-H19-N-O2
209
Vasodilator, peripheric
Benzenemethanol, α-[(butylamino)methyl]-4-hydroxy-
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 |
| OS | Official Synonym |
| PH | Pharmacopoeia Name |
| Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
| USAN | United States Adopted Name |
Cocarboxylasa may be available in the countries listed below.
Cocarboxylase hydrochloride (a derivative of Cocarboxylase) is reported as an ingredient of Cocarboxylasa in the following countries:
International Drug Name Search
Loctin may be available in the countries listed below.
Lovastatin is reported as an ingredient of Loctin in the following countries:
International Drug Name Search
Alfaciclina may be available in the countries listed below.
Tetracycline hydrochloride (a derivative of Tetracycline) is reported as an ingredient of Alfaciclina in the following countries:
International Drug Name Search
Frovatex may be available in the countries listed below.
Frovatriptan is reported as an ingredient of Frovatex in the following countries:
International Drug Name Search
Thrombodine may be available in the countries listed below.
Ticlopidine hydrochloride (a derivative of Ticlopidine) is reported as an ingredient of Thrombodine in the following countries:
International Drug Name Search
Ceftazidima Mylan may be available in the countries listed below.
Ceftazidime pentahydrate (a derivative of Ceftazidime) is reported as an ingredient of Ceftazidima Mylan in the following countries:
International Drug Name Search
Berberin Domesco may be available in the countries listed below.
Berberine chloride hydrate (a derivative of Berberine) is reported as an ingredient of Berberin Domesco in the following countries:
International Drug Name Search
Prednisolone EG may be available in the countries listed below.
Prednisolone 21-(sodium 3-sulfobenzoate) (a derivative of Prednisolone) is reported as an ingredient of Prednisolone EG in the following countries:
International Drug Name Search
Ceftriaxon Hikma may be available in the countries listed below.
Ceftriaxone disodium salt (a derivative of Ceftriaxone) is reported as an ingredient of Ceftriaxon Hikma in the following countries:
International Drug Name Search
Esdelart may be available in the countries listed below.
Danazol is reported as an ingredient of Esdelart in the following countries:
International Drug Name Search
Azitromicina Generis may be available in the countries listed below.
Azithromycin is reported as an ingredient of Azitromicina Generis in the following countries:
International Drug Name Search
Codidol may be available in the countries listed below.
Dihydrocodeine tartrate (a derivative of Dihydrocodeine) is reported as an ingredient of Codidol in the following countries:
International Drug Name Search
Xorim may be available in the countries listed below.
Cefuroxime sodium salt (a derivative of Cefuroxime) is reported as an ingredient of Xorim in the following countries:
International Drug Name Search
Captopril Pharmagenus may be available in the countries listed below.
Captopril is reported as an ingredient of Captopril Pharmagenus in the following countries:
International Drug Name Search
Biotclarcin may be available in the countries listed below.
Clarithromycin is reported as an ingredient of Biotclarcin in the following countries:
International Drug Name Search
