INDORAMIN is a brand name for Indoramin. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Conditions for which alpha blockade is indicated. Management of urinary outflow obstruction due to benign prostatic hyperplasia.
Verbatim from this product's MHRA label. Tap a section to expand.
Posology Hyperplasia Adults: 20 mg twice daily. Dosage may be increased in 20 mg increments at two-weekly intervals up to max. 100 mg per day if required. Elderly: 20 mg at night may be adequate.
Paediatric population:
Not recommended. Method of administration For oral administration.
Drowsiness or sedation can occur on starting treatment with indoramin, and also if dosage is increased too rapidly. Less commonly, dry mouth, nasal congestion, weight gain, dizziness, failure of ejaculation, depression, fatigue, headache and hypotension (including postural hypotension) with or without syncope may occur.
Rarely, Parkinson's disease could be exacerbated. Rarely, hypersensitivity reactions including rash and pruritus may occur. Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important.
It allows continued monitoring of the benefit/risk balance of the medicinal product. uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Incipient cardiac failure should be controlled before treatment with indoramin. Caution should be observed in prescribing indoramin for patients with hepatic or renal insufficiency. A few cases of extrapyramidal disorders have been reported in patients treated with indoramin.
Caution should be observed in prescribing indoramin in patients with Parkinson's disease. In animals and in the one reported case of overdose in humans, convulsions have occurred. Due consideration should be given, and great caution exercised in the use of indoramin in patients with epilepsy.
The 'Intraoperative Floppy Iris Syndrome (IFIS, a variant of small pupil syndrome) has been observed during cataract surgery in some patients on or previously treated with tamsulosin. Isolated reports have also been received with other alpha-1 blockers and the possibility of a class effect cannot be excluded.
As IFIS may lead to increased procedural complications during the cataract operation current or part use of alpha-1 blockers should be made known to the ophthalmic surgeon in advance of surgery. Caution should be observed in prescribing indoramin for patients with a history of depression.
Clearance of indoramin may be affected in the elderly. A reduced dose, and/or reduced frequency of dosing may be sufficient in some elderly patients. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
1 Patients with established heart failure. Patients already under treatment with a monoamine oxidase inhibitor.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Indoramin in United Kingdom.
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Brand names are compiled from public regulatory records for active-ingredient mapping only. Drugvu is not affiliated with any manufacturer. This is not medical advice.