trenbolone acetate

Trenbolone acetate has antipyretic and analgesic effect due to blockade of the cyclooxygenase in the central nervous system and the effects on pain centers and thermoregulation. Inflammatory drug, has anti-inflammatory, analgesic and antipyretic effect associated with nonselective inhibition of cyclooxygenase activity, which regulates the synthesis of prostaglandins .

Caffeine – causes dilation of blood vessels in skeletal muscle, heart, kidney; enhances mental and physical performance, helps to eliminate fatigue and drowsiness; gistogematicheskih increases the permeability barriers and enhances the bioavailability of non-narcotic analgesics, thereby enhancing the therapeutic effect. It has a tonic effect on the brain vessels.

Drotaverine – myotropic exerts a spasmolytic effect due to inhibition of phosphodiesterase IV, acts on the smooth muscle in the gastrointestinal tract, biliary tract, urinary and cardiovascular systems.

Pheniramine – blocker of H1-histamine receptors. It has antispasmodic and mild sedative effect, reduces the phenomenon of exudation, but also enhances the analgesic effects of acetaminophen and naproxen.

Indications
Pain syndrome of different genesis, including pain in the joints, muscles, sciatica, menstrual pain, neuralgia, toothache and headaches (including headaches, caused by a spasm of cerebral vessels).

Pain associated with spasm of smooth muscles, including those with chronic cholecystitis, cholelithiasis, postcholecystectomy syndrome, renal colic.

Posttraumatic and postoperative trenbolone acetate pain, including accompanied by inflammation.

Colds accompanied by a feverish syndrome (as a symptomatic therapy).

Contraindications
: Hypersensitivity to the drug, erosive and ulcerative lesions of the gastrointestinal tract (exacerbation), gastrointestinal bleeding, complete or incomplete combination of bronchial asthma, recurrent nasal polyposis, and paranasal sinuses and intolerance of aspirin or other nonsteroidal anti-inflammatory drugs, including a history of severe hepatic and / or renal failure, inhibition of bone marrow hematopoiesis, condition after coronary artery bypass surgery; heavy organic diseases of the cardiovascular system (including acute myocardial infarction), paroxysmal tachycardia, frequent ventricular premature beats, severe arterial hypertension, hyperkalemia, children under 18 years, pregnancy and lactation.

Be wary – cerebrovascular disease, diabetes mellitus, peripheral arterial disease, ulcerative lesions of the gastrointestinal tract in history, renal and liver failure, mild or moderate severity, viral hepatitis, alcoholic liver disease, benign hyperbilirubinemia (Gilbert’s syndrome, Dubin-Johnson and Rotor ), epilepsy and susceptibility to seizures, lack of glucose-6-phosphate dehydrogenase, old age.

If you have one of these diseases / conditions before taking this medication, you should consult with your doctor.

Dosing and Administration

Inside. The drug is taken 1 tablet 1-3 times a day. The maximum daily dose – 4 tablets.

Duration of treatment is not more than 3 days as antipyretic and not more than 5 days – as an analgesic. Continuation of treatment is possible only after consultation with your doctor. Do not exceed this dose!

Side effects:
Allergic reactions: skin rash, pruritus, urticaria, angioedema;

From the side of hematopoiesis: trenbolone acetate thrombocytopenia, leukopenia, agranulocytosis, anemia, methemoglobinemia;

From the nervous system: agitation, anxiety, increased reflexes, tremor, headache, sleep disturbances, dizziness, decreased concentration;

Since the cardiovascular system: heart rate, arrhythmia, increased blood pressure;

From the digestive system: erosive and ulcerative lesions of the gastrointestinal tract, nausea, vomiting, epigastric discomfort, abdominal pain, constipation, abnormal liver function; Anastrozole side effects, anastrozole 1 mg bodybuilding anastrozole for men.