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Composition:
Active ingredient: gabapentin 300 mg
Description:
300 mg: opaque yellow hard gelatin capsules, size 1.
Capsule contents: white powder.
Dosage form
300 mg capsules. 10 capsules
per blister, 2 or 5 blisters per cardboard box with instructions for use. Pharmacological action: The exact mechanism of action is unknown. Gabapentin's chemical structure is similar to that of the neurotransmitter gamma-aminobutyric acid (GABA), but its mechanism of action differs from other drugs that interact with GABA receptors. See full instructions for medical use. Indications for Use: Treatment of neuropathic pain in adults 18 years of age and older. Monotherapy of partial seizures with or without secondary generalization in adults and children aged 12 years and older. As an adjunct to treatment of partial seizures with or without secondary generalization in adults and children aged 3 years and older. Method of Administration: Orally, with or without food. If it is necessary to reduce the dose, discontinue the drug; this should be done gradually over at least one week. Neuropathic pain in adults: the initial dose of Gabagamma® is 900 mg/day given in three equal doses; if necessary, the dose is gradually increased to a maximum of 3600 mg/day. It should be taken into account that no additional efficacy was observed with gabapentin at doses higher than 1800 mg per day. Treatment can be started immediately with a dose of 900 mg/day (300 mg 3 times a day), or the dose can be gradually increased to 900 mg per day over the first 3 days according to the following regimen: Day 1: 300 mg of the drug once a day; Day 2: 300 mg 2 times a day; Day 3: 300 mg 3 times a day. For the treatment of epilepsy - See full instructions.
Patients with renal insufficiency require a reduced dose of gabapentin - see instructions for medical use. Interaction: see instructions for medical use. Side Effects: Very common and common: leukopenia, infections; anorexia, increased appetite; hostility, confusion, emotional lability, depression, anxiety, increased nervous excitability; drowsiness, dizziness, ataxia; visual disturbances, hypertension, vasodilation; nausea, vomiting, diarrhea, abdominal pain, dyspepsia, constipation, dry mouth and throat, flatulence; Facial swelling, hemorrhagic rash, most often described as bruising due to physical trauma, rash, itching, acne; joint pain, muscle pain, back pain, twitching; fatigue, fever; peripheral edema, gait disturbances, asthenia, pain in various locations. See full instructions. Contraindications: Hypersensitivity to any component of the drug, lactose intolerance, lactase deficiency, glucose-galactose malabsorption. Treatment of neuropathic pain in children and adolescents under 18 years of age.
Use during pregnancy and breastfeeding: There are no data on the use of gabapentin in pregnant women. The risk associated with epilepsy and antiepileptic drugs should be assessed. The effect of gabapentin on breastfed infants is unknown. See package insert. Overdose: See package insert. Special Instructions: Effect on Ability to Drive
and Operate Machines
Driving or operating potentially dangerous machinery is not recommended while taking this medication until the absence of a negative impact on these functions has been confirmed. Gabapentin affects the central nervous system and can cause dizziness, drowsiness, confusion, loss of consciousness, and other CNS symptoms. Even if mild or moderate, these adverse reactions can pose a risk to patients driving
vehicles or operating other machinery. This risk is especially high at the beginning of treatment or after increasing the dose.
See package insert.
READ THE FULL INSTRUCTIONS BEFORE USE!
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