Glucomet Plus tablet 5/500 mg 60’s

what are the adverse effects of Glucomet Plus tablet 5/500 mg 60’s?

Transient visual disturbances occur at the start of treatment. Very common: Nausea, vomiting, diarrhoea, abdominal pain & loss of appetite. Common: Taste disturbances. Uncommon: Crises of hepatic porphyria & porphyria cutanea; average to moderate elevations of serum urea & creatinine conc. Rare: Leukopenia, thrombocytopenia, pruritus urticaria, maculopapular rash. Very rare: Agranulocytosis, haemolytic anaemia, bone marrow aplasia & pancytopenia; lactic acidosis; liver function test abnormality or hepatitis requiring withdrawals of treatment; cutaneous or visceral allergic angiitis, erythema multiforme, exfoliative dermatitis, photo-sensitization, urticaria evolving to shock & cross-sensitivity to sulphonamides.

What happens if I miss a dose of Glucomet Plus tablet 5/500 mg 60’s?

Adults: Initial therapy, 250 mg/1.25 mg once daily.
Patients with fasting glucose gt; 200 mg/dL: May start with 250 mg/1.25 mg twice daily. Dosage may be increased in increments of 250 mg/1.25 mg at intervals of not less than 2 wk; max daily dose 2000 mg/10 mg.
Previously treated with a sulphonylurea or metformin alone: Initial 500 mg/2.5 mg or 500 mg/5 mg twice daily, increase in increments no greater than 500 mg/5 mg; max daily dose 2000 mg/20 mg.
Children: Not recommended.

One of the following licensed pharmacy from the nearest location will deliver Glucomet Plus tablet 5/500 mg 60’s. The details of the licensed pharmacy shall be shared once you request the drugs and the respective pharmacy accepts your request based on valid prescription and availability.