Pregnancy, myasthenia gravis, liver testosterone enanthate powder dysfunction and mild-moderate renal dysfunction of mild to moderate severity , elderly patients; in patients with congenital or acquired prolongation receiving therapy antiarrhythmics of classes cisapride, with hypokalemia or hypomagnesemia, clinically significant bradycardia, arrhythmia or severe heart failure; concurrent use of terfenadine, warfarin, digoxin, diabetes mellitus; simultaneous application of cyclosporine, antipsychotics such as pimozide; antidepressants such as citalopram; and fluoroquinolones such as moxifloxacin and levofloxacin.
Application of pregnancy and during breastfeeding
Application of the drug during pregnancy is possible only when the intended benefits to the mother outweighs the potential risk to the fetus.
If necessary, the appointment during lactation should stop breastfeeding (excreted in breast milk).
Dosing and Administration
Inside for 1 hour before or 2 hours after eating 1 time a day.
After taking the drug the child must always be asked to drink a few sips of water, so that he can swallow the remains of the suspension.
Prior to each administration of the drug vial contents thoroughly stirred until a homogeneous suspension. If the required volume of suspension was not selected from the vial for 20 min after shaking, the suspension should be shaken again to select the required volume and to the child.
The desired dose is metered by syringe to dispense with division value 1 ml nested in the carton together with the vial.
When pharyngitis / tonsillitis, caused by testosterone enanthate powder pyogenes, the drug is used at a dose of 20 mg / kg / day for 3 days (course dose 60 mg / kg).
The maximum daily dose is 500 mg. When Lyme disease (initial stage of Lyme disease) – erythema migrans (Erythema migrans): in the first day at a dose of 20 mg / kg / day, and then with the 2nd to the 5th day in a dose of 10 mg / kg / day (course dose 60 mg / kg).
Patients with impaired function kidney: when used in patients with impaired renal mild to moderate severity function (creatinine clearance 40 mL / min) dose adjustment is required. patients with impaired hepatic function: when applied in patients with disorders of mild to moderate liver functions of degree of gravity dose adjustment is required. In elderly patients, a dose adjustment is required. A method for preparing a suspension suspension 100 mg / 5 mL: you need to carefully shake the dry powder. The powder was added 10.0 ml of purified water. For the introduction of the syringe tip is placed into the neck of the bottle, while cap must be opened. To the vial contents intended for the preparation of 20 ml of the suspension (nominal volume) with a syringe for dispensing 10 ml of water. Agitated until a homogeneous suspension. The volume of the suspension obtained be about 25 ml, which exceeds the nominal volume of approximately 5 ml. This is provided to compensate for the inevitable loss of the suspension at the dosing of the drug. The suspension can be stored at a temperature no higher than 30 ° C for up to 5 days. The suspension 200 mg / 5 mL: you need to carefully shake the dry powder. To the contents of the vial, intended for preparation of 15 ml suspension (nominal volume) with a syringe to dispense 7.5 ml of water. Agitated until a homogeneous suspension. The volume of the resulting suspension to about 20 ml, which exceeds the nominal volume of approximately 5 ml.
This is provided to compensate for testosterone enanthate powder the inevitable loss of the suspension at the dosing of the drug. The suspension can be stored at a temperature no higher than 30 ° C for up to 5 days. The powder is added to water, the following: – For 15 ml (600 mg) (reconstituted suspension) are added 7.5 ml of water – for 20 ml (800 mg) (recovered slurry) was added 10.0 ml of water – for 22.5 mL (900 mg) (recovered slurry) was added 11.0 ml of water – for 30 ml (1200 mg) (recovered slurry) was added 15.0 ml of water – to 37.5 ml (1500 mg) (recovered slurry) was added 18.5 ml of water.
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