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An important advantage of semi-synthetic macrolides is a longer half-life, which allows them to be administered 1-2 times a day.

With normal renal function, T 1/2 for erythromycin is 2-3 hours, for clarithromycin 5-7 hours, 10-20 hours for roxithromycin, and for azithromycin more than 48 hours. Macrolides are used to treat infections of the upper and lower respiratory tract (pneumonia, bronchitis, pharyngitis, acute sinusitis), diphtheria, scarlet fever, whooping cough, otitis media, infections of the skin, soft tissues, pelvic organs, oral cavity, sexually transmitted infections, and eradication of Helicobacter pylori in peptic ulcer, for the purpose of year-round prevention of rheumatism . Rp.: Cilasaprili 0.0005 (0.001; 0.0025; 0.005) Pharmachologic effect Overdose pastae Zinci ad 10.0 110. twenty Table eleven Preventive and therapeutic efficacy of the systemic use of the drug is manifested in Meniere's disease, the main clinical symptoms of which include bouts of dizziness (vertigo) with nausea and vomiting; noise in ears.

Do not apply to open wounds, mucous membranes, the area of the purulent process.

For adults, the dose at the start of treatment should be 20–60 mg and should be titrated according to thyroid function until the patient is euthyroid to reduce the risk of overtreatment and consequent hypothyroidism. As part of complex therapy for varicose veins with edematous and pain syndromes, superficial thrombophlebitis, trophic disorders and ulcers, Buy Hytrin (Terazosin hydrochloride) 1mg, 2mg, 5mg online - Blood Pressure with chronic venous insufficiency, with hemorrhagic diathesis.

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as operating towels and napkins. Rational prevention of caries in children should begin from infancy and continue throughout the entire period of eruption of milk and permanent teeth. Adults are usually prescribed 1 mg 3-4 times a day for resorption in the oral cavity. Children

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4-6 years - 3 times a day, 0.5 mg; 7-18 years - 4 times a day, 0.5 mg.

Sodium fluoride is used between meals, holding the tablets in the mouth until completely dissolved, swallowing saliva.

Accepted for 200-250 days a year with a break in the summer. Intramuscular 2 ml 1–3 times in day from ten november 1997 G. 326 Ketamine (ketalar ¤ ) is a non-competitive antagonist of N - methyl - D -aspartate receptors ( NMDA receptors), has a pronounced analgesic effect. Estrogen, intended for the treatment of patients with symptoms of estrogen deficiency and complications of menopause. Cyanocobalamini pro injectionibus 200 mkg - 1 ml Appoint from 1/4 _ _ before one tab. 3–5 once in day after food, in dependencies from age.

1.0 Antitussive drugs are shown, with a slight broncholi- tic action, drugs that thin the mucus bronchi (expectorants) preparations): Pregnant women and women during lactation: 1 tablet 1-2 times a day.

Dosage and administration For normalization microcirculation use- ut rheopolyglucin (rec.

Rp.: Orthopheni 0.025 (0.05) Hypersensitivity to diphenhydramine.

The lozenge should be kept in the mouth until completely dissolved.

Adults and children over 4 years: 1 lozenge every 3-4 hours.

5 SCROLL Pharmachologic effect Pharmachologic effect Release form: tablets of 0.1 and 0.2 g; 5 ml ampoules of 1% solution. Rp.: Vikasoli 0.015 Indications for use Hydrocortisone With endocrine disorders - in case of acute insufficiency of the adrenal cortex; in preparation for surgery or in case of severe injury/disease in patients with adrenal insufficiency or insufficient adrenocortical reserve.

Degranol (mannomustine) ampoules Among anti-tuberculosis drugs, an antibacterial group is distinguished: rifampicin, streptomycin, kanamycin, amikacin, viomycin (florimycin sulfate ? Hypersensitivity to the drug, liver disease in the acute phase, a steady increase in serum transaminase activity, pregnancy and lactation, porphyria, age up to 18 years. Also use official drugs: The analgesic effect is additionally mediated through the influence on adrenergic and serotonergic transmission (neuronal uptake of norepinephrine and serotonin

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in the descending antinociceptive pathways is impaired), resulting in increased descending inhibitory effects on the conduction of pain impulses at the level of the spinal cord.