Each sustained-release, film-coated tablet contains:
Alfuzosin hydrochloride …….........................…...............................………………………... 5 mg
Excipients …..................................................... q.s. ad to one sustained-release, film-coated tablet
Nexavar® 200 mg film-coated tablets.
Qualitative and quantitative composition: 200 mg sorafenib (as tosylate)
Warnings and Precautions: Hand-foot skin reaction and rash, usually CTC grade 1 and 2. Increased incidence of arterial hypertension (usually mild to moderate, early in the course of treatment). Blood pressure should be monitored regularly and treated as appropriate. Increased risk of bleeding. Increased incidence of cardiac ischaemia/infarction. Use sorafenib with caution in patients who may have, or may develop prolongation of QTc, and consider periodic monitoring (on-treatment electrocardiograms, electrolytes). Gastrointestinal perforation in less than 1%; sorafenib to be discontinued. Levels of sorafenib may be increased in patients with severe hepatic impairment. Infrequent bleeding events or elevations in INR have been reported in some patients taking warfarin concomitantly. Patients on such therapy should be monitored. Temporary treatment interruption and/or dose modification or discontinuation may be considered, depending on the severity of the observed adverse reactions. No formal studies on wound healing have been conducted. Temporary interruption of sorafenib therapy is recommended in patients undergoing major surgical procedures. In elderly cases of renal failure have been reported. High risk patients according to MSKCC prognostic group were not included in the phase III study in renal cell carcinoma and benefit-risk has not been evaluated in these patients. Caution is recommended when administering sorafenib with compounds that are metabolised/eliminated predominantly by the UGT1A1 (e.g. irinotecan) or UGT1A9 pathways. Caution is recommended when sorafenib is co-administered with docetaxel. The risk of reduced plasma concentrations of sorafenib should be considered before starting a treatment course with antibiotics. Higher mortality has been reported in patients with squamous cell carcinoma of the lung with sorafenib in combination with platinum-based chemotherapies. Due to the potential risk of bleeding, tracheal, bronchial, and oesophageal infiltration should be treated with localized therapy prior to administering sorafenib in patients with differentiated thyroid cancer (DTC). When using sorafenib in patients with DTC, close monitoring of blood calcium level is recommended. Severe hypocalcaemia should be corrected to prevent complications such as QT-prolongation or torsade de pointes. When using sorafenib in DTC patients, close monitoring of TSH level is recommended.
Undesirable effects: Very common: infection, lymphopenia, anorexia, hypophosphataemia, haemorrhage (incl. gastrointestinal, respiratory tract, cerebral), hypertension, diarrhoea, nausea, vomiting, constipation, dry skin, rash, alopecia, hand-foot skin reaction (palmar plantar erythrodysaesthesia syndrome), erythema, pruritus, arthralgia, fatigue, pain (mouth, abdominal, bone, tumour, headache), fever, weight decreased, increased amylase and lipase. Common: folliculitis, leucopenia, neutropenia, anaemia, thrombocytopenia, hypothyroidism, hypocalcaemia, hypokalaemia, hyponatraemia, depression, peripheral sensory neuropathy, dysgeusia, tinnitus, congestive heart failure, myocardial ischemia and infarction, flushing, rhinorrhea, dysphonia, stomatitis (including dry mouth and glossodynia), dyspepsia, dysphagia, gastro oesophageal reflux disease, keratoacanthoma / squamous cell cancer of the skin, dermatitis exfoliative, acne, skin desquamation, hyperkeratosis, myalgia, muscle spasms, renal failure, proteinuria, erectile dysfunction, asthenia, influenza like illness, mucosal inflammation, transient increase in transaminases. Uncommon: hypersensitivity reactions (including skin reactions and urticaria), anaphylactic reaction, hyperthyroidism, dehydration, reversible posterior leukoencephalopathy, hypertensive crisis, interstitial lung disease–like events (pneumonitis, radiation pneumonitis, acute respiratory distress, etc), pancreatitis, gastritis, gastrointestinal perforations, increase in bilirubin, jaundice, cholecystitis, cholangitis, eczema, erythema multiforme, gynaecomastia, increase in alkaline phosphatase, INR abnormality, prothrombin level abnormality. Rare: Angioedema, QT prolongation, drug induced hepatitis, radiation recall dermatitis, Stevens-Johnson syndrome, rhabdomyolysis, nephrotic syndrome, toxic epidermal necrolysis, leucocytoclastic vasculitis.
Amaryl 1mg Tablet: Each tablet contains 1mg glimepiride, as active ingredient.
Amaryl 2mg Tablet: Each tablet contains 2mg glimepiride, as active ingredient.
Amaryl 3mg Tablet: Each tablet contains 3mg glimepiride, as active ingredient.
Amaryl 4mg Tablet: Each tablet contains 4mg glimepiride, as active ingredient.
Lactose, sodium starch glycolate, polyvidone 25000, microcrystalline cellulose,
magnesium stearate, red ferric oxide (Amaryl 1.0), yellow ferric oxide (Amaryl
2.0 and Amaryl 3.0), indigo carmine aluminium lake (Amaryl 2.0 and Amaryl 4.0).
Glimepiride, the active ingredient of Amaryl, is a blood-sugar-lowering agent belonging
to the sulfonylurea group. The decrease in blood sugar is achieved principally by
means of the stimulation of insulin release from pancreatic beta cells. This effect is
predominantly based on improved responsiveness of these cells to the physiological
glucose stimulus. Glimepiride augments the normal action of insulin on peripheral
glucose uptake. Moreover, it mimics such action as well as the glucose output of the
liver. Good metabolic control over 24 hours can be achieved with a single dose of
In patients with insufficient response to the maximum dose, combined use with an
additional oral antidiabetic containing metformin or with insulin improves metabolic
Non-insulin-dependent (type II) diabetes, whenever blood sugar levels cannot be
controlled adequately by diet, physical exercise and weight reduction alone. Amaryl
may also be used in combination with an oral antidiabetic containing metformin or
Strictly follow the recommended dosage unless directed otherwise by the physician.
In principle, the dosage of Amaryl is governed by the desired blood sugar level. The
dosage of glimepiride must be the lowest which is sufficient to achieve the desired
Treatment with Amaryl must be initiated and monitored by a physician. Amaryl must
be taken at the times and in the doses prescribed. Mistakes, e.g. forgetting to take a
dose, must never be corrected by subsequently taking a larger dose. Measures for
dealing with such mistakes (in particular forgetting a dose or skipping a meal) or
situations where a dose cannot be taken at the prescribed time must be discussed
and agreed between physician and patient beforehand. A physician must be notified
immediately if the dose taken is too high, or an extra dose has been taken.
The initial and the maintenance doses are set based on the results of regular checks
of glucose in blood and urine. Monitoring of glucose levels in blood and urine also
serves to detect either primary or secondary failure of therapy.
Initial dose and dose titration: The usual initial dose is 1mg Amaryl once daily. If
necessary, the daily dose can be increased. Any increase should be based on regular
blood sugar monitoring, and should be gradual, i.e., at intervals of one to two weeks,
and carried out stepwise, as follows: 1mg - 2mg - 3mg - 4mg - 6mg, and in exceptional
Dose range in patients with well controlled diabetes: The usual dose range in
patients with well controlled diabetes is 1 to 4 mg Amaryl daily. Only some patients
benefit from daily doses of more than 6 mg.
Distribution of doses: Timing and distribution of doses are to be decided by the
physician, taking into consideration the patient's current life-style. Normally, a single
daily dose of Amaryl is sufficient. This dose should be taken immediately before a
substantial breakfast or- if none is taken- immediately before the first main meal. It
is very important not to skip meals after taking Amaryl.
Secondary dosage adjustment: As the control of diabetes improves, sensitivity to
insulin increases; therefore, glimepiride requirements may fall as treatment proceeds.
To avoid an excessive reduction in blood sugar (hypoglycaemia), a timely dose
reduction or cessation of Amaryl therapy must be considered.
A dose adjustment must also be considered whenever the patient's weight or lifestyle
changes, or other factors causing an increased susceptibility to hypoglycaemia
or to an excessive increase in blood sugar levels (hyperglycaemia) arise (see under
"Warnings and precautions").
Duration of treatment:
Treatment with Amaryl is normally a long-term therapy.
Changeover from other oral antidiabetics to Amaryl: There is no exact dosage
relationship between Amaryl and other oral blood-sugar-lowering agents. When substituting
Amaryl for other such agents, the initial daily dose is 1 mg; this applies even
in changeovers from the maximum dose of another oral blood-sugar-lowering agent.
Any Amaryl dose increase should be in accordance with guidelines given above in
"Initial dose and dose titration".
Consideration must be given to the potency and duration of action of the previous
blood-sugar-lowering agent. It may be necessary to interrupt treatment to avoid
additive effects which would increase the risk of hypoglycaemia.
Use in combination with metformin: Whenever blood sugar levels cannot be controlled
adequately with the maximum daily dose of either Amaryl or a metformin-containing
antidiabetic alone, both medicines may be used concomitantly. In such cases,
the dose of the established medicine remains unchanged. Treatment with the additional
medicine is started at a low dose, which - depending on the desired blood
sugar level - may then be increased gradually up to the maximum daily dose. Combined
treatment should be initiated under close medical supervision.
Use in combination with insulin: Whenever blood sugar levels cannot be controlled
adequately with the maximum daily dose of Amaryl, insulin may be given concomitantly.
In this case, the current dose of Amaryl remains unchanged. Insulin treatment
is started at a low dose, which is subsequently increased stepwise according to
the desired blood sugar level. Combined treatment should be initiated under close
Special Populations Renal Insufficiency: There is limited information available on
the use of Amaryl in renal insufficiency. Patients with impaired renal function may
be more sensitive to the glucose-lowering effect of Amaryl.
Amaryl tablets must be swallowed without chewing and with sufficient amounts of
liquid (approximately. 1/2 glass).
Amaryl is not suitable for the treatment of insulin-dependent (type I) diabetes mellitus
(e.g., for the treatment of diabetics with a history of ketoacidosis), of diabetic
ketoacidosis, or of diabetic precoma or coma.
Amaryl must not be used in patients hypersensitive to glimepiride, other sulfonylureas,
other sulfonamides, or to any of the excipients (see "Composition").
No experience has been gained concerning the use of Amaryl in patients with severe
impairment of liver function and in dialysis patients. In patients with severe impairment
of hepatic function, changeover to insulin is indicated, not least to achieve
optimal metabolic control.
Pregnancy and lactation: To avoid risk of harm to the child, Amaryl must not be
taken during pregnancy; a changeover to insulin is necessary. Patients planning a
pregnancy must inform their physician, and should change over to insulin.
Ingestion of glimepiride with the breast milk may harm the child. Therefore, Amaryl
must not be taken by breast-feeding women, and a changeover to insulin or discontinuation
of breast-feeding is necessary.
Warnings and precautions
To achieve optimal control of blood sugar, a correct diet, regular and sufficient physical
exercises and, if necessary, reduction of body weight are just as important as regular
intake of Amaryl. Clinical signs of hyperglycaemia are, e.g., increased urinary
frequency, intense thirst, dryness of the mouth, and dry skin.
When starting treatment, the patient must be informed about the effects and risks of
Amaryl and about its role in conjunction with dietary measures and physical exercise;
the importance of adequate co-operation must also be stressed.
In the initial weeks of treatment, the risk of hypoglycaemia may be increased and
necessitates especially careful monitoring. Factors favouring hypoglycaemia include:
-unwillingness or (more commonly in older patients) incapacity of the patient to
- under nutrition, irregular mealtimes, or skipped meals,
- imbalance between physical exertion and carbohydrate intake,
- alterations of diet
- consumption of alcohol, especially in combination with skipped meals,
- impaired renal function,
- severe impairment of liver function,
- overdosage with Amaryl,
- certain uncompensated disorders of the endocrine system affecting carbohydrate
metabolism or counter-regulation of hypoglycaemia (as, for example, in certain disorders
of Thyroid function and in anterior pituitary or adrenocortical insufficiency),
- concurrent administration of certain other medicines (see "Interactions").
The physician must be informed about such factors and about hypoglycaemic episodes,
since these require particularly careful monitoring.
If such risk factors for hypoglycaemia are present, it may be necessary to adjust the
dosage of Amaryl or the entire therapy. This also applies whenever illness occurs during
therapy or the patient's life-style changes. Those symptoms of hypoglycaemia
which reflect the body's adrenergic counter-regulation (see under "Adverse effects")
may be milder or absent in those situations where hypoglycaemia develops gradually,
in the elderly, and in patients with a certain type of nervous disease (autonomic
neuropathy) or those receiving concurrent treatment with beta-blockers, clonidine,
reserpine, guanethidine, or other sympatholytic medicines.
Hypoglycaemia can almost always be promptly controlled by immediate intake of
sugar, e.g., in the form of glucose, sugar cubes or sugar-sweetened beverages.
Patients should always carry at least 20 grams of glucose with them for this purpose
(food or beverages containing artificial sweeteners - such as diet foods or drinks - are
ineffective in controlling hypoglycaemia). They may require the assistance of other
persons to avoid complications.
It is known from other sulfonylureas that, despite initially successful countermeasures,
hypoglycaemia may recur. Therefore, continued close observation is necessary.
Severe hypoglycaemia requires, in addition, immediate treatment and follow-up by a
physician and, in some circumstances, hospitalisation.
If treated by different physicians (upon, e.g., admission to hospital after an accident,
illness while on holiday), the patients must inform them about their diabetes and
In exceptional stress situations (e.g., trauma, surgery, infections with fever) blood
sugar control may deteriorate, and a temporary change to insulin may be necessary.
During treatment with Amaryl, glucose levels in blood and urine must be checked
regularly, as should, additionally, the proportion of glycated haemoglobin.
Alertness and reactions may be impaired due to hypo- or hyperglycaemia, especially
when beginning or after altering treatment, or when Amaryl is not taken regularly.
Such impairement may, for example, affect the ability to operate a vehicle or machinery.
Amaryl overdose may lead to severe and sometimes life-threatening hypoglycaemia
and may require hospitalisation even as a precautionary measure. Significant overdose
with severe reactions is a medical emergency and will necessitate immediate
treatment and hospitalisation.
Mild episodes of hypoglycaemia can usually be treated with oral carbohydrates.
Adjustments in dosage, meal patterns or physical activity may be necessary. More
severe episodes with coma, seizure or neurologic impairment may be treated with
glucagon (intramuscular or subcutaneous) or concentrated glucose solution (intravenous).
If life-threatening amounts have been ingested, detoxification (by, e.g., gastric
lavage, activated charcoal) will be necessary.
Sustained administration of carbohydrates and observation may be necessary
because hypoglycaemia may recur after apparent clinical recovery.
In order to avoid possible interactions with other medicines, inform your physician or
pharmacist about any other current treatment.
Patients who take or discontinue taking certain other medicines while undergoing
treatment with Amaryl may experience changes in blood sugar control.
Based on experience with Amaryl and on what is known of other sulfonylureas, the
following interactions must be considered:
Potentiation of the blood-sugar-lowering effect and, thus, in some instances hypoglycaemia
may occur when one of the following medicines is taken, for example: insu-
lin and other, oral Antidiabetics, ACE inhibitors, allopurinol, anabolic steroids and
male-sex-hormones, chloramphenicol, coumarin derivatives, cyclophosphamide, disopyramide,
fenfluramine, fenyramidol, fibrates, fluoxetine, guanethidine, isofosfamide,
MAO-inhibitors, miconazole, para-aminosalicylic acid, pentoxifylline (high dose
parenteral), phenylbutazone, azapropazone, oxyphenbutazone, probenecid, quinolones,
salicylates, sulfinpyrazone, sulfonamides, tetracyclines, tritoqualine, trofosfamide.
Weakening of the blood-sugar-lowering effect and, thus, raised blood sugar levels
may occur when one of the following medicines is taken, for example: acetazolamide,
barbiturates, corticosteroids, diazoxide, diuretics, epinephrine (adrenaline) and
other sympathomimetic agents, glucagon, laxatives (after protracted use), nicotinic
acid (in high doses), oestrogens and progestogens, phenothiazines, phenytoin, rifampicin,
H2 receptor antagonists, clonidine and reserpine may lead to either potentiation or
weakening of the blood-sugar-lowering effect.
Beta-blockers decrease glucose tolerance. In patients with diabetes mellitus, this may
lead to deterioration of metabolic control. In addition, beta-blockers may increase
the tendency to hypoglycaemia (due to impaired counter-regulation).
Under the influence of sympatholytic medicines such as beta-blockers, clonidine,
guanethidine and reserpine, the signs of adrenergic counter-regulation to hypoglycaemia
may be reduced or absent.
Both acute and chronic alcohol intake may potentiate or weakens the blood-sugarlowering
action of Amaryl unpredictably.
The effect of coumarin derivatives may be potentiated or weakened.
Please tell your physician or pharmacist if you experience any adverse effect with the
use of Amaryl.
Based on experience with Amaryl and on what is known of other sulfonylureas, the
following adverse effects must be considered:
Hypoglycaemia: As a result of the blood-sugar-lowering action of Amaryl, hypoglycaemia
may occur, and may also be prolonged.
Possible symptoms of hypoglycaemia include headache, ravenous hunger, nausea,
vomiting, lassitude, sleepiness, disordered sleep, restlessness, aggressiveness,
impaired concentration, alertness and reactions, depression, confusion, difficulty in
speaking and even speech loss, visual disorders, tremor, pareses, sensory disturbances,
dizziness, helplessness, loss of self-control, delirium, cerebral convulsions, somnolence
and loss of consciousness up to and including coma, shallow respiration and
slow heart rate (bradycardia). In addition, signs of adrenergic counter-regulation may
be present such as sweating, clammy skin, anxiety, rapid heart rate (tachycardia),
hypertension, palpitations, angina pectoris, and cardiac arrhythmias. The clinical picture
of a severe hypoglycaemic attack may resemble that of a stroke. The symptoms
of hypoglycaemia nearly always subside when hypoglycaemia is corrected.
Eyes: Especially at the start of treatment, temporary visual impairment may occur
due to the change in blood sugar levels.
Digestive tract: Occasionally, gastrointestinal symptoms such as the following may
occur:nausea, vomiting, sensations of pressure or fullness in the epigastrium,
abdominal pain, and diarrhoea.
In rare cases, liver enzyme levels may increase. In isolated cases, impairment of liver
function (e.g. with cholestasis and jaundice) and hepatitis may develop, possibly
leading to liver failure.
Blood: Severe changes in the blood picture may occur: Rarely, thrombopenia and, in
isolated cases, leucopenia, haemolytic anaemia or, e.g. erythrocytopenia, granulocytopenia,
agranulocytosis, and pancytopenia (e.g. due to myelosuppression) may
Other adverse reactions: Occasionally, allergic or pseudoallergic reactions may
occur, e.g. in the form of itching, urticaria or rashes. Such reactions may be mild, but
also may become more serious and may be accompanied by dyspnoea and a fall in
blood pressure, sometimes progressing to shock. If urticaria occurs, a physician must
be notified immediately.
In isolated cases, a decrease in serum sodium, inflammation of blood vessels (allergic
vasculitis) and hypersensitivity of the skin to light may occur.
Since some adverse effects (e.g., severe hypoglycaemia, certain changes in the blood
picture, severe allergic or pseudoallergic reactions, or liver failure) may under certain
circumstances become life-threatening, it is essential that, if sudden or severe reactions
do occur, you inform a physician at once, and on no account continue taking
the drug without a physician's express guidance.
Storage: Do not store above 25°C
Expiry Date: Do not use later than the date of expiry.
Keep medicines out of the reach of children.
Amaryl 1mg Tablets: Pack of 2 x 10 Tablets.
Amaryl 2mg Tablets: Pack of 2 x 10 Tablets.
Amaryl 3mg Tablets: Pack of 2 x 10 Tablets.
Amaryl 4mg Tablets: Pack of 2 x 10 Tablets.
HYTRIN 1,2,3,4 mg
Ingredient(s):Each tablet contains Terazosin HCl 1,2,3,4 mg
Indications :To relieve the signs & symptoms of Benign Prostatic Hyperplasia(BPH). Also used alone or in combination with other antihypertensive agents for treatment of hypertension.
Ingredient(s): Each 5ml emulsion contains:
Magnesium Hydroxide Mixture………. 3.5ml
Liquid Paraffin ……………………… 1.25ml Indications : Constipation
Ingredient(s): Each sachet contains:
Sodium Bicarbonate…... ... ... 1.716 gm
Sodium Citrate ……. ... . ... ... 0.613 gm
Citric Acid ... ... ... ………... ...0.702 gm
Tartaric Acid ... ... ... ... .….. ... 0.858 gm Indications : Condition where long term or short term maintenance of alkaline urine is desirable. In condition where temporary relief from minor gastric upsets is desired. In combination with antibiotics; when the effectiveness of an antibiotic is increased in the presence of alkaline urine.
Ingredient(s): Each Cofcol tablet or each tablespoon (15ml) of Cofcol Elixir provides:
Pseudoephedrine HCl ...........30 mg
Chlorpheniramine maleate...........1 mg
Dextromethorphan HBr ...........10 mg
Vitamin C ......................50 mg Indications: COFCOL tablets and elixir are indicated for both adults and children for the relief of the following symptoms associated with influenza, colds, allergies, and other upper respiratory disorders:
CECON ® DROPS
Ingredients: Each ml. contains 100 mg of vitamin C in a vehicle of propylene glycol. Indications: CECON Drops is indicated as a dietary supplement of vitamin C for infants & children.
Cecon®-500 Chewable Tablets
Ingredients: Each Cecon® chewable tablet contains 500 mg of ascorbic acid. Indications: Each Cecon chewable tablet is indicated whenever ascorbic acid is required in greater than average doses for the prevention and treatment of ascorbic acid deficiency. Ascorbic acid deficiency results in scurvy. Collagenous structures are primarily affected, and lesions develop in bones and blood vessels. Administration of ascorbic acid completely reverses the symptoms of ascorbic acid deficiency. In addition to the therapy of overt deficiency conditions, such as adult and infantile scurvy, ascorbic acid is used as an adjunctive agent in the treatment of such conditions as:
Ingredient(s): Each 100gm contains Euflavine 0.1gm w/w Indications : For Treatment of Burns, Cuts, Wounds, Abrasions, Simple Suppurating or Tropical sores, and Infective Skin conditions.
BRUFEN TABLET 200MG
Ingredient(s): Each tablet contains:
Ibuprofen : 200 mg Indications: Rheumatoid arthritis including juvenile rheumatoid arthritis or still's disease, ankylosing spondylitis, osteoarthritis, other non-rheumatoid (seronegative) arthropathies and acute gouty arthritis and periarticular conditions such as frozen shoulder (capsulitis), bursitis, tendonitis, tenosynovitis and low-back pain. Soft tissue injuries. Mild to moderate pain such as dysmenorrhoea, dental and post operative pain. Symptomatic relief of headache including migraine headache.
BRUFEN TABLET 400MG
Ingredient(s): Each tablet contains:
Ibuprofen : 400 mg Indications: Rheumatoid arthritis including juvenile rheumatoid arthritis or still's disease, ankylosing spondylitis, osteoarthritis, other non-rheumatoid (seronegative) arthropathies and acute gouty arthritis and periarticular conditions such as frozen shoulder (capsulitis), bursitis, tendonitis, tenosynovitis and low-back pain. Soft tissue injuries. Mild to moderate pain such as dysmenorrhoea, dental and post operative pain. Symptomatic relief of headache including migraine headache.
Ingredient(s): Each 5 ml contains:
Ibuprofen : 100 mg
In an orange flavoured syrupy base Indications: Brufen suspension exhibits potent antipyretic, analegesic and anti inflammatory, properties with a wide margin of safety. It is therefore indicated in pyrexia associated with upper respiratory tract infections and other disorders. Juvenile rheumatoid arthritis soft tissue inflammation, traumatic inflammation, non specific aches.
Ingredient(s): Per 100gm
Ibuprofen : 10 gm Indications: For treatment of bruises, sprains, muscular pain, strain, pain in joints and muscles, lumbago, tenosynovitis, phlebitis and similar conditions.
Composition(s): Each ml contains
Ingredients Bejectal and Bejectal-T Vitamin B1 10mg 100mg Vitamin B2 2mg 2mg Vitamin B6 5mg 5mg Nicotinamide 75mg 75mg Dexpanthenol 5mg 5mg
Indications: To prevent deficiencies of or to meet the increased requirements for the water-soluble vitamins in conditions where ingestion, gastrointestinal absorption or utilization is impaired. Examples of conditions which may require parenteral administration of these vitamins in order to rapidly restore tissue levels are the following: hyperemesis gravidarum, chronic diarrhoea, chronic diseases complicated by inadequate dietary deficiency as in chronic alcoholism, many postoperative states including those involving delayed healing, especially of the gastrointestinal tract, and other situations requiring parenteral feeding.
Composition(s): Each Tablet contains:
Thiamine HCl ( B1 ) 100 mg
Pyridoxine HCl ( B6) 50 mg
Cyanocobalamin ( B12) 50 mcg Indications: Bevidox is indicated as a vitamin supplement in the treatment of vitamin B1 , B6 , and B12 deficiency
Ingredient(s): Each Becefol tablet provides the following ingredients: Composition & Dosage Vitamin C750 mg Nicotinamide100 mg Vitamin E .30 IU Calcium pantothenate20 mg Vitamin B1 (Thiamine)15 mg Vitamin B2 (Riboflavin)10 mg Vitamin B6 (Pyridoxine hydrochloride)5 mg Vitamin B124 mcg Folic Acid150 mcg Indications: BECEFOL filmtab vitamin tablets are indicated as a nutritional supplement where there is an inadequate intake of these vitamins in patients with either poor eating habits or increased vitamin requirements.
Ingredient(s): Each 10ml vial contains:
Acyclovir Sodium equivalent to Acyclovir 500mg Indications: Acyclovir is indicated for the treatment of:
Ingredient(s): Each effervescent tablet contains :
Calcium carbonate .....670 mg (equivalent to 268 mg of elemental calcium)
Vitamin D .....400 I.U.
Vitamin C .....500 mg.
Vitamin B6 .....10.0 mg. Indications:
Pack Size: 10s in aluminium tube
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