Примери за използване на Janumet на Английски и техните преводи на Български
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What Janumet contains.
How to take Janumet 4.
Janumet should be taken.
How to store Janumet 6.
Janumet is taken twice a day.
Before you take Janumet 3.
Janumet 50 mg/ 850 mg film-coated tablets.
Other medicines and Janumet.
Janumet is contraindicated in patients with.
Medication name Janumet.
Blister for Janumet 50 mg/ 850 mg film-coated tablets.
If you stop taking Janumet.
Outer carton for Janumet 50 mg/ 850 mg film-coated tablets.
Do not take a double dose of Janumet.
If you stop taking Janumet, your blood sugar may rise again.
If you forget to take Janumet.
Janumet contains two different medicines called sitagliptin and metformin.
The name of your tablet is Janumet.
Janumet 50 mg/ 850 mg film-coated tablets sitagliptin/ metformin hydrochloride.
No animal studies have been conducted with Janumet.
If acute pancreatitis is confirmed, Janumet should not be restarted.
No data are available with regard to overdose of Janumet.
Continue to take Janumet as long as your doctor prescribes it so you can continue to help control your blood sugar.
For patients switching from co-administration of sitagliptin and metformin For patients switching from co-administration of sitagliptin and metformin, Janumet should be initiated at the dose of sitagliptin and metformin already being taken.
If a hypersensitivity reaction is suspected,discontinue Janumet, assess for other potential causes of the event, and institute alternative treatment for diabetes(see section 4.8).
During post-marketing experience of Janumet or sitagliptin, one of the active substances of Janumet,  the following additional adverse reactions have been reported(frequency not known): hypersensitivity reactions including anaphylaxis, angioedema, rash, urticaria, and exfoliative skin conditions including Stevens-Johnson syndrome(see section 4.4).
For patients switching from co-administration of sitagliptin and metformin, Janumet should be initiated at the dose of sitagliptin and metformin already being taken.
If a hypersensitivity reaction is suspected, Janumet should be discontinued, other potential causes of the event should be assessed, and alternative treatment for diabetes should be instituted(see section 4.8).
Change in clinical status of patients with previously controlled type 2 diabetes A patient with type 2 diabetes previously well controlled on Janumet who develops laboratory abnormalities or clinical illness(especially vague and poorly defined illness) should be evaluated promptly for evidence of ketoacidosis or lactic acidosis.
A patient with type 2 diabetes previously well controlled on Janumet who develops laboratory abnormalities or clinical illness(especially vague and poorly defined illness) should be evaluated promptly for evidence of ketoacidosis or lactic acidosis.