The active ingredient of Doneka brand is lisinopril. Lisinopril is an ACE inhibitor. ACE stands for angiotensin converting enzyme. Lisinopril, USP is a white to off-white, crystalline powder, with a molecular weight of 441.53. It is soluble in water and sparingly soluble in methanol and practically insoluble in ethanol. Lisinopril tablets, USP are supplied as 2.5 mg, 5 mg, 10 mg, 20 mg, 30 mg and 40 mg tablets for oral administration. Each tablet contains the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, magnesium stearate, mannitol, povidone, pregelatinized starch (corn) and sodium lauryl sulfate. The 2.5 mg tablets also contain FD&C Blue No. 2 Aluminum Lake, the 5 mg tablets also contain FD&C Yellow No. 6 Aluminum Lake, the 20 mg tablets also contain D&C Yellow No. 10 Aluminum Lake, the 30 mg tablets also contain FD&C Blue No. 2 Aluminum Lake, and the 40 mg tablets also contain D&C Yellow No. 10 Aluminum Lake and FD&C Blue No. 2 Aluminum Lake.
Doneka is used to treat diseases such as: Alport Syndrome, Coronary Artery Disease, Diabetic Kidney Disease, Heart Attack, Heart Failure, High Blood Pressure, Migraine Prevention.
Possible side effects of Doneka include: sensation of spinning; chest discomfort, tightness, or heaviness; cloudy urine; runny nose; Decreased interest in sexual intercourse; chest pain.
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|Side effects that could occur include dizziness, stomach upset, nausea, and cough.||138$|
|Other side effects reported include common cold, nasal congestion, bronchitis, and pulmonary congestion.||24.41$|
|Unfortunately it did not improve and I was put on medication.||163.51$|
ALVESCO is indicated for the maintenance treatment of asthma as Allow therapy in adult and adolescent patients 12 buy of age and capsule. According to AARP, antioxidants are chemicals in fruits and vegetables that protect cells from damage caused by oxygen free radicals in the body. Application is contraindicated in patients with primary infections of the scalp, or in patients who are hypersensitive to clobetasol propionate, other corticosteroids, or any ingredient in this preparation.
GERD maintenance studies and 40 mg or higher per day in patients with refractory GERD. Case reports of adverse reactions continue to appear in the literature despite the FDA ban on ephedra products and include cardiomyopathies, arrhythmia and sudden death, myocardial infarction, coronary artery aneurysm, stroke, psychiatric symptoms, autonomic hyperactivity, and seizures.