PHENYLEPHRINE is a brand name for Phenylephrine. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Phenylephrine Injection is indicated in adults and children for the treatment of hypotensive states e.g. circulatory failure, during spinal anaesthesia or drug induced hypotension.
Verbatim from this product's MHRA label. Tap a section to expand.
1% solution, repeated as necessary after at least 15 minutes. 9% injection may be infused intravenously, initially at a rate of up to 180 micrograms per minute, reduced according to response to 30-60 micrograms per minute. Elderly There is no need for dosage reduction in the elderly.
Paediatric population 100 mcg/kg body weight subcutaneously or intramuscularly. Method of administration For subcutaneous, intramuscular, slow intravenous injection or intravenous infusion.
A tabulated list of undesirable effects is outlined below:
The undesirable effects are listed according to organ systems and following frequency: Not known (cannot be estimated from the available data) System organ class Undesirable effects Immune system disorders Hypersensitivity Metabolism and nutrition disorders Metabolic disorders Psychiatric disorders Nervousness, insomnia Nervous system disorders Headache, cerebral haemorrhage, paraesthesia Eye disorders Mydriasis, angle-closure glaucoma Cardiac disorders Pulmonary oedema, bradycardia, tachycardia, arrhythmia, angina pectoris, palpitations, cardiac arrest Vascular disorders Hypotension, dizziness, syncope, flushing Respiratory, thoracic and mediastinal disorders Dyspnoea Gastrointestinal disorders Vomiting, salivary hypersecretion Renal and urinary disorders Dysuria, urinary retention General disorders and administration site conditions Extravasation, infusion site necrosis, hyperhidrosis Investigations Increased blood pressure, abnormal blood glucose Phenylephrine is without significant stimulating effects on the central nervous system at usual doses.
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.
Great care should be exercised in administering Phenylephrine Injection to patients with pre-existing cardiovascular disease such as ischaemic heart disease, arrhythmias, occlusive vascular disease including arteriosclerosis, hypertension or aneurysms.
Anginal pain may be precipitated in patients with angina pectoris. Care is also required when given to patients with diabetes mellitus. Phenylephrine is not recommended in subjects with a shallow anterior chamber or a history of acute narrow angle glaucoma.
Use of Phenylephrine 10 mg/ml Injection in patients with shallow anterior chamber, a history of acute narrow angle glaucoma and/or insufficient pupil dilation can increase the risk of both iridocele and floppy iris syndrome. Keep all medicines out of the reach of children.
This medicine contains less than 1 mmol sodium (23 mg) per ml, that is to say essentially ‘sodium-free’.
1. Patients taking monoamine oxidase inhibitors, or within 14 days of ceasing such treatment. Severe hypertension and hyperthyroidism. Avoid in patients with prostatic enlargement.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Phenylephrine 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.
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