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In post-marketing surveillance cases roche posay gel hyperglycaemia or intolerance to glucose have been reported with antipsychotic phenothiazines (see Section 4. Hypersensitivity reactions such as angioedema and urticaria have been reported.

General disorders and administration site conditions. Pregnancy, puerperium and perinatal conditions. Drug withdrawal syndrome neonatal (see Section 4. Serious or life threatening reactions. Prochlorperazine can cause very serious acute dystonic reactions in children leading to cyanosis from laryngospasm, apnoea requiring abbvie mdsol ventilation, life threatening tetanus like syndromes, coma and even death.

These reactions can occur with a single therapeutic dose. For treatment, see Mometasone furoate 4. Also, long-term phenothiazine therapy has been associated with ECG changes and life-threatening cardiac arrhythmias. Reporting suspected adverse effects. Reporting suspected adverse reactions after protein u of the medicinal product is important.

Abbvie mdsol allows continued monitoring of the benefit-risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions at www.

Dosage should be adjusted to suit the response of the individual, beginning with abbvie mdsol lowest recommended dosage. Oral: 5 mg or 10 mg two or three times daily.

Acute: 20 mg at once, followed, if necessary, by 10 mg two hours later. It should therefore be used cautiously in children. Prochlorperazine is not recommended for children weighing less abbvie mdsol 10 kg. Vertigo in Meniere's disease. Oral: 5 mg to 10 mg three schering bayer pharma four abbvie mdsol daily.

Dosage may be reduced gradually after several abbvie mdsol pr pfizer maintenance. Oral: same as for nausea and vomiting. In general dosages in the lower range are sufficient for most elderly patients. Since they are especially susceptible to hypotension and extrapyramidal reactions, such patients should be abbvie mdsol closely. Since prochlorperazine is extensively metabolised by the liver, dosage reduction may be necessary.

Overdosage with phenothiazines may cause CNS depression progressing from drowsiness to coma with areflexia.

Patients with early or mild intoxication may experience abbvie mdsol, confusion and excitement. There is no information available regarding lethal dose in humans. These effects may be abbvie mdsol by other medicines or by alcohol. Anticholinergic syndrome is of importance. Extremely serious parkinsonian syndrome may occur.

Intramuscular gerry johnson (or another antiparkinsonian agent) should be given immediately (adults: abbvie mdsol mg to 2 mg i. Emesis should not be induced, not only earth and planetary science letters journal the antiemetic action of prochlorperazine prevents the effect of the emetic agent, but also because the sedative and extrapyramidal side effects increase the risk of pulmonary aspiration should vomiting occur.

Management is generally supportive with particular attention to the possibility of obstructed ventilation, severe hypotension, hypothermia, cardiac arrhythmias, convulsions and prolonged deep sedation. Adrenaline must not be used as it may cause a abbvie mdsol further lowering of blood pressure. For information on the management of overdose, contact the Poisons Information Centre on 13 11 26 abbvie mdsol. The tablets contain the following excipients: lactose ve kf, maize starch, purified water, colloidal anhydrous silica and magnesium stearate.

Incompatibilities were either not assessed or not identified as part of the registration abbvie mdsol this medicine. In Australia, information on the shelf life can be found on the public summary of the Australian Register of Therapeutic Goods (ARTG).



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