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Benzamycin (Erythromycin)- FDA

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Immediate hypersensitivity reactions may occur after administration of ipratropium bromide solution as demonstrated by rare cases of urticaria (including giant urticaria), pruritus, angioedema of Benzamycin (Erythromycin)- FDA tongue, lips and face, laryngospasm and rash. Acute angle closure glaucoma following direct eye contact, an anticholinergic side effect has been reported rarely. If the substance enters the eyes by inappropriate handling, mild and reversible disturbance of accommodation may occur.

Other ocular complications have also summer cold reported, including, mydriasis, increased intraocular pressure, eye pain. Urinary retention, an anticholinergic side effect has been reported rarely. The risk of urinary retention may be increased in patients Benzamycin (Erythromycin)- FDA pre-existing outflow tract obstruction.

APO-Ipratropium can be administered via a range of commercially available nebulising devices. Dosage is dependent on the mode of inhalation and the nebuliser used and should be adjusted to suit individual patient requirements.

Daily doses exceeding 2 mg in adults and 1 mg in children under 12 years of age should be given Benzamycin (Erythromycin)- FDA medical supervision. If the response to the treatment is inadequate, medical advice should be sought so that appropriate measures Benzamycin (Erythromycin)- FDA be taken. It is advisable not to greatly exceed the recommended daily dose as this suggests additional therapeutic modalities may be needed.

The recommended dosage is 250 to 500 microgram, diluted to 2 to 3 mL with normal saline and nebulised until the entire volume of solution is inhaled, every 6 hours. In cases of Dipivefrin (Propine)- FDA bronchospasm or with assisted ventilation, a dose in the lower range of 1 mL (250 microgram) is recommended.

In more severely distressed patients, 500 microgram has been shown to produce optimal bronchodilatation. Inhalation may be repeated after 2 hours. A dose of 250 microgram diluted to 2 to 3 mL with Benzamycin (Erythromycin)- FDA saline is recommended for children under 12 years of age, administered in the Benzamycin (Erythromycin)- FDA way as for adults.

The effects of this medicine on a person's ability to drive and use machines were not assessed as part of its registration.

Accidental overdose by inhalation Benzamycin (Erythromycin)- FDA unlikely. Single doses of ipratropium 30 mg by mouth (equivalent to sixty 2 mL vials of APO-Ipratropium 0. No symptoms specific Benzamycin (Erythromycin)- FDA overdosage have Suboxone (Buprenorphine HCl and naloxone HCl)- FDA encountered.

In view of the wide therapeutic range and topical administration of ipratropium bromide Benzamycin (Erythromycin)- FDA solutions, no serious anticholinergic symptoms are to be expected. Minor systemic manifestations of anticholinergic action, including dry mouth, visual accommodation disturbances and tachycardia may occur.

For information on the management of overdose, contact the Poison Information Centre on 131126 (Australia). Incompatibilities were either not assessed or not identified as part of the registration of this medicine. In Australia, any unused medicine or waste material should be disposed of by taking to your local pharmacy.

Reasonable care is taken to provide accurate information at the time of creation. This information is not intended as a substitute for medical advice and should not be exclusively relied on Benzamycin (Erythromycin)- FDA manage or diagnose a medical condition. NPS MedicineWise disclaims all liability (including for negligence) for any loss, damage or injury resulting from reliance on or use of this information.

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