primobolan depot

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Treatment of type 2 diabetes in middle-aged and elderly patients (with the poor diet)


  • type 1 diabetes,
  • diabetic ketoacidosis, precoma, coma;
  • Hypersensitivity to sulfonylureas or sulfonamides;
  • pregnancy, breastfeeding.

Dosage and administration
is necessary to strictly observe the advice of a doctor to normalize glucose metabolism in the patient. You should not stop treatment on their own, without telling your doctor. The initial dose is usually Primobolan depota ½ tablets (15 mg) at breakfast. If necessary, increase the dose gradually, according to the doctor’s recommendations.
Increasing the dose to 4 tablets (120 mg) a day usually does not lead to a further intensification of the effect.

When replacing oral hypoglycemic agents with a similar mechanism of action starting dose is determined depending on the disease at the time of drug administration. The initial dose is typically ½ -1 tablet (15-30 mg). The dose is increased only on doctor’s advice.
If Primobolan depota daily dose does not exceed 2 tablets (60 mg), it can be administered at one time, during breakfast. However, the best effect is achieved when administering the drug 2-3 times a day.Primobolan depot should be taken with food, at the beginning of the meal.

Side effects
Rare: hypoglycemic reactions, allergic skin reactions, changes in blood system and disorders of the gastrointestinal tract.

Possible hypoglycemic states, disorders of the gastrointestinal tract. In the case of a hypoglycemic condition requires immediate administration of glucose orally or intravenously.

Interactions with other drugs
salicylates, sulfonamides, derivatives phenylbutazone, anti-TB drugs, chloramphenicol, tetracyclines and coumarin derivatives, cyclophosphamide, MAO inhibitors and β-blockers, may increase the hypoglycemic effect of sulfonylureas.
May decrease hypoglycemic action, while the appointment Primobolan depota and chlorpromazine, sympathomimetic , glyukortikosteroidov, thyroid hormone, and oral contraceptive preparations containing niacin.
Primobolan depot may reduce alcohol tolerance.

Although Primobolan depot excreted in the urine in small amounts (5%), and is generally well tolerated in renal disease, treatment of patients with severe renal insufficiency should be under close medical supervision.
In case of pregnancy, you should stop taking the drug and consult a doctor immediately. If necessary, use during breast-feeding, breast-feeding should be discontinued.

Patients with diabetes are prone to develop cardiovascular disorders. The risk can be reduced only with strict adherence to the prescribed diet. Oral hypoglycemic agents should not replace medical diet that allows you to monitor the patient’s body weight and is mandatory regardless of the use of a drug. All oral hypoglycemic agents at untimely meal or non-recommended dosing regimen may lead to a significant reduction in blood glucose levels and the loss of ability to concentrate. The use of sugar, sweets or sugary drinks usually helps prevent starting hypoglycemic reaction. In the case of persistent hypoglycemic condition should consult a doctor immediately.

In case of sickness during treatment Primobolan depotom (fever, rash, nausea) should immediately seek medical advice.
In case of allergic reactions, you should stop taking Primobolan depota, replacing it with other hypoglycemic agents or insulin.

Effects on ability to drive vehicles and management mechanisms
In the period of dose adjustment or change the drug should avoid activities potentially hazardous activities that require increased attention and psychomotor speed reactions.

Storage conditions
In a dry place at a temperature no higher than 25 ° C. Keep out of reach of children!

Product Form
The tablets of 30 mg. 10 tablets in blister packs.
In 3.6 or 12 blisters with instruction on use is placed in a cardboard box. shop steroids tamoxifen citrate bodybuilding anti estrogens & fat loss