GALPSEUD LINCTUS is a brand name for Pseudoephedrine. The medicine, its uses, side effects and dosage are the same regardless of brand.
Used for: Indicated for the relief of nasal, sinus and upper respiratory congestion.
Verbatim from this product's MHRA label. Tap a section to expand.
For oral administration.
Adults and children over 12 years:
Two 5ml spoonfuls three times daily. Children: 6-12 years: 5ml three or four times daily.
Elderly:
Adult dose is appropriate.
The following side effects may be associated with the use of pseudoephedrine: (frequencies not known: cannot be estimated from the available data).
Immune system disorders:
Hypersensitivity reactions – cross-sensitivity may occur with other sympathomimetics.
Psychiatric disorders:
Hallucinations (particularly in children), insomnia, sleep disturbances, anxiety, restlessness, irritability, excitability, psychotic disorder has occurred rarely following misuse of pseudoephedrine.
Nervous system disorders:
Headache, tremor, dry mouth.
Eye disorders:
Angle-closure glaucoma.
Ischaemic optic neuropathy Cardiac disorders:
Tachycardia, palpitations, arrhythmia.
Vascular disorders:
Hypertension, impaired circulation to the extremities.
Gastrointestinal disorders:
Nausea, vomiting, ischaemic colitis.
Skin and subcutaneous tissue disorders:
Fixed drug eruption in the form of erythematous nodular patches, rash. Severe skin reactions, including acute generalized exanthematous pustulosis (AGEP).
Renal and urinary disorders:
Urinary retention. 4. 4. 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.
Caution should be used in prescribing Galpseud Linctus for patients with prostatic enlargement or bladder dysfunction. Also use with caution in patients with severe hepatic impairment, or with mild to moderate renal impairment. If any of the following occur, Galpseud Linctus should be stopped • Hallucinations • Restlessness • Sleep disturbances.
• Excipient warnings: This medicine contains Amaranth (E123), Sunset Yellow (E110) and Sodium hydroxybenzoates (E215, E217 & E219) which may cause allergic reactions (possibly delayed). 9% v/v. The amount of ethanol in 5ml of this medicine is equivalent to less than 2ml of beer and 1ml of wine.
The small amount of alcohol in this medicine will not have any noticeable effects. This medicine contains less than 1mmol sodium (23mg) per 5ml dose, that is to say essentially ‘sodium-free’. Severe Skin reactions Severe skin reactions such as acute generalized exanthematous pustulosis (AGEP) may occur with pseudoephedrine-containing products.
This acute pustular eruption may occur within the first 2 days of treatment, with fever, and numerous, small, mostly non-follicular pustules arising on a widespread oedematous erythema and mainly localized on the skin folds, trunk, and upper extremities.
Patients should be carefully monitored. If signs and symptoms such as pyrexia, erythema, or many small pustules are observed, administration of Galpseud Linctus should be discontinued and appropriate measures taken if needed. Ischaemic colitis Some cases of ischaemic colitis have been reported with pseudoephedrine.
Pseudoephedrine should be discontinued and medical advice sought if sudden abdominal pain, rectal bleeding or other symptoms of ischaemic colitis develop. Ischaemic optic neuropathy Cases of ischaemic optic neuropathy have been reported with pseudoephedrine.
Pseudoephedrine should be discontinued if sudden loss of vision or decreased visual acuity such as scotoma occurs. 8). 3). Pseudoephedrine should be discontinued and immediate medical assistance sought if the following symptoms occur: sudden severe headache or thunderclap headache, nausea, vomiting, confusion, seizures and/or visual disturbances.
Galpseud Linctus should not be used in patients hypersensitive to pseudoephedrine, or any of the other ingredients. Patients receiving monoamine oxidase inhibitors or who have received these agents in the last two weeks. Patients using other sympathomimetic decongestants or beta-blockers.
5). Patients with cardiovascular disease including ischaemic heart disease, occlusive vascular disease and hypertension. Children under 6 years of age. Patients with: • Severe renal impairment • Phaeochromocytoma • Diabetes • Hyperthyroidism • Closed angle glaucoma • Severe hypertension or uncontrolled hypertension • Severe acute or chronic kidney disease/renal failure.
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
Other brands of Pseudoephedrine in United Kingdom.
Know a brand we are missing in United Kingdom? Suggest a brand →
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.
uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.
Most reported cases of PRES and RCVS resolved following discontinuation and appropriate treatment. Do not exceed the stated dose. Keep out of the sight and reach of children.