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Phenergan is treating different types of allergy symptoms, including itching, runny nose, sneezing, itchy or watery eyes, hives, and itchy skin rashes.

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Generic Phenergan Information

Introduction

Phenergan is a widely used medication in the United Kingdom for the relief of allergic symptoms, nausea, and motion‑induced discomfort. Its active ingredient is promethazine, a first‑generation antihistamine that belongs to the allergy drug group. Although the original brand was introduced by Sanofi‑Aventis, the compound is now available from many manufacturers in both brand‑name and generic forms. In addition to its primary anti‑allergic action, Phenergan is prescribed for pre‑operative sedation, treatment of postoperative nausea and vomiting (PONV), and as an adjunct in cough suppression.

What is Phenergan?

Phenergan is a brand name for the antihistamine promethazine hydrochloride. Promethazine was first synthesized in the 194s and introduced as an antihistamine that also possesses strong sedative and anti‑emetic properties. The medication is marketed in several dosage forms, including oral tablets (12.5 mg, 25 mg), syrup, rectal suppositories, and injectable solutions (25 mg ml⁻¹).

While Phenerga ® is the original trade name, the same active compound is sold under other well‑known brand names such as Promethegan, Dicaine, and Promethazine Hydrochloride. Generic promethazine tablets contain the identical molecule and are therapeutically equivalent, offering a lower‑cost alternative for patients who require long‑term or intermittent treatment.

How Phenergan Works

Promethazine exerts its therapeutic effects through several pharmacological actions:

  • Histamine H₁‑receptor antagonism – By blocking H₁ receptors in peripheral tissues, the drug prevents the cascade that leads to vasodilation, edema, and itching characteristic of allergic reactions.
  • Central anticholinergic activity – In the brainstem, promethazine inhibits muscarinic receptors, reducing the vestibular input that triggers motion‑induced nausea.
  • Sedative property via central dopamine antagonism – The compound mildly blocks dopamine D₂ receptors, contributing to its calming effect and making it useful for pre‑operative sedation.

The onset of action after oral administration is typically 30 minutes, with peak plasma concentrations reached within 2–4 hours. The elimination half‑life ranges from 10 to 20 hours, allowing once‑daily dosing for chronic indications while still providing adequate coverage for acute symptoms.

Conditions Treated with Phenergan

  • Allergic rhinitis and urticaria – Histamine release from mast cells is curtailed, relieving sneezing, rhinorrhea, and hives.
  • Motion sickness – Central anticholinergic effects suppress the vestibular signals that provoke nausea in travelers.
  • Nausea and vomiting (including postoperative) – Promethazine’s anti‑emetic action diminishes gastrointestinal motility and the chemoreceptor trigger zone response.
  • Pre‑operative sedation – A single oral or intramuscular dose produces calming, anxiolytic effects prior to surgery.
  • Cough associated with upper‑respiratory infections – The sedative component can reduce cough reflex sensitivity.

In the UK, allergic diseases affect roughly 30 % of adults each year, while postoperative nausea impacts up to 70 % of surgical patients without prophylaxis. Phenergan’s multimodal activity addresses these prevalent clinical challenges.

Who is Phenergan For?

Phenergan is appropriate for adult patients who require relief from moderate to severe allergic symptoms, nausea related to motion or postoperative states, or a short‑acting sedative before minor procedures. It is especially useful when a single agent can address both histamine‑mediated itching and accompanying nausea.

Contra‑indications include:

  • Known hypersensitivity to promethazine or any phenothiazine derivatives.
  • Severe hepatic impairment (Child‑Pugh class C).
  • Concurrent use of monoamine oxidase inhibitors (MAOIs) or other potent central nervous system depressants without careful monitoring.

Caution is advised in elderly patients (> 65 years) because of an increased risk of sedation, orthostatic hypotension, and anticholinergic side‑effects such as urinary retention or constipation.

Risks, Side Effects, and Interactions

Common

  • Drowsiness or sedation
  • Dry mouth and throat
  • Blurred vision due to cycloplegia
  • Constipation

Rare

  • Extrapyramidal symptoms (e.g., tremor, rigidity)
  • Photosensitivity reactions
  • Hypotension, especially when standing quickly

Serious

  • Severe allergic reaction (anaphylaxis) – facial swelling, bronchospasm, rapid pulse
  • Neuroleptic malignant syndrome – high fever, muscle rigidity, autonomic instability
  • Respiratory depression in patients with compromised airway reflexes

Drug‑Drug Interactions

  • CNS depressants (opioids, benzodiazepines, alcohol) → additive sedation, possible respiratory depression.
  • Anticholinergic agents (e.g., atropine, antihistamine combinations) → increased risk of dry mouth, urinary retention, and confusion.
  • MAO inhibitors → heightened risk of hypertensive crisis and serotonin syndrome when combined with serotonergic agents.
  • QT‑prolonging drugs (e.g., macrolide antibiotics, certain antipsychotics) → additive effect on cardiac repolarisation; ECG monitoring recommended in high‑risk patients.

Patients should provide their pharmacist or healthcare professional with a complete list of current medicines, including over‑the‑counter products and herbal supplements.

Practical Use: Dosing, Missed Dose, Overdose

Standard adult dosing (oral)

  • Allergic reactions: 12.5 mg to 25 mg every 4–6 hours as needed; maximum 100 mg per day.
  • Motion sickness: 25 mg taken 30 minutes before travel; repeat every 4–6 hours if required.
  • Post‑operative nausea: 12.5 mg to 25 mg every 6 hours; administered intravenously or intramuscularly if oral route is unsuitable.

Missed dose – If a scheduled dose is forgotten, take it as soon as remembered provided there is at least a 4‑hour gap before the next dose. Do not double‑dose to compensate for the missed tablet.

Overdose – Symptoms may include extreme drowsiness, confusion, seizures, or cardiac arrhythmias. Immediate medical attention is essential. Gastric lavage or activated charcoal may be considered by emergency clinicians if presentation is within one hour of ingestion.

Practical precautions

  • Avoid alcohol and other sedatives while taking Phenergan, as they amplify central nervous system depression.
  • Do not operate heavy machinery or drive until the individual’s response to the medication is known.
  • Patients with glaucoma, enlarged prostate, or urinary retention should discuss the anticholinergic risk with a clinician before use.
  • For patients with hepatic disease, dose reduction (e.g., 12.5 mg every 6–8 hours) may be necessary due to prolonged clearance.

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Patients who encounter limited stock, high costs, or insurance barriers can consider our pharmacy as a cost‑effective, trustworthy alternative.

FAQ

  • Can Phenergan be taken with other antihistamines?
    Combining Phenergan with additional antihistamines may increase sedation and anticholinergic​‑related side effects. It is generally discouraged unless directed by a clinician who can monitor for excessive drowsiness.

  • Is there a difference between the tablet and syrup formulations?
    Both contain the same amount of promethazine per dose; however, the syrup uses liquid excipients that may be preferable for patients with difficulty swallowing tablets. The syrup also allows finer dose adjustments for weight‑based pediatric use (though pediatric dosing is outside the scope of this adult‑focused article).

  • How should Phenergan be stored in a hot climate?
    Store the product at a controlled room temperature of 15 °C – 30 °C, away from direct sunlight and humidity. In consistently hot environments, keep the medication in a cool, insulated container to protect the active ingredient from degradation.

  • Does Phenergan appear on standard drug‑testing panels?
    Promethazine is not typically screened for in routine workplace or sports drug tests, as it is not classified as a performance‑enhancing or illicit substance.

  • Are there specific warnings for patients of Asian descent?
    No ethnic‑specific contraindications have been identified for promethazine. However, certain populations may have a higher prevalence of the CYP2D6 poor‑metabolizer phenotype, potentially leading to increased plasma levels; dose adjustments should be considered under clinical supervision.

  • Can Phenergan be used in pregnancy?
    Promethazine is classified as Category B (UK) – animal studies have not shown fetal risk, but there are insufficient human data. It should only be used during pregnancy when clearly needed and after a risk‑benefit assessment by a qualified health professional.

  • What packaging does Phenergan come in when ordered online?
    Tablets are supplied in sealed, printed blister packs of 30 units each. Injectable vials arrive in tamper‑evident amber glass bottles, each containing 5 ml of solution. All shipments include a printed information leaflet in English.

  • Can Phenergan be imported for personal use without a prescription?
    Personal import of prescription‑only medicines into the UK is allowed under the MHRA’s “personal importation scheme” provided that the quantity does not exceed a three‑month supply and the individual holds a valid prescription from a qualified prescriber.

  • Are there notable differences between UK‑licensed and US‑licensed promethazine products?
    The active ingredient and potency are identical, but excipient profiles may vary (e.g., different binding agents or preservatives). UK formulations must comply with the European Pharmacopoeia standards, while US products follow the USP monograph.

  • What is the history behind the development of promethazine?
    Promethazine was first synthesized by scientists at the Rhône‑Poulenc laboratory in 1949 as part of a series of phenothiazine derivatives. It received approval in the early 195s for allergy relief and was subsequently repurposed for anti‑nausea and sedative uses, leading to the commercial brand Phenergan.

  • How does promethazine compare with newer antihistamines like cetirizine?
    Promethazine has broader pharmacologic activity, including significant sedation and anti‑emetic effects, whereas cetirizine is a second‑generation antihistamine with minimal central nervous system penetration and therefore less drowsiness. Choice of agent depends on the therapeutic goal—sedation and nausea control favor promethazine, while daytime allergy relief without sedation favors cetirizine.

Glossary

Anticholinergic
A property of a drug that blocks the action of the neurotransmitter acetylcholine at muscarinic receptors, often leading to dry mouth, dilated pupils, and reduced gastrointestinal motility.
Phenothiazine
A chemical class that includes promethazine and several antipsychotic agents; characterised by a tricyclic structure that confers antihistamine and sedative activity.
First‑generation antihistamine
An older class of H₁‑receptor blockers that readily cross the blood‑brain barrier, producing both peripheral anti‑allergic effects and central sedation.
Neuroleptic malignant syndrome
A rare but life‑threatening reaction to dopamine‑blocking drugs, marked by hyperthermia, muscle rigidity, autonomic instability, and altered mental status.

⚠️ Disclaimer

The information provided about Phenergan is for general knowledge only. It does not replace professional medical consultation. All treatment decisions should be made under the supervision of a qualified healthcare provider. We assume all readers are responsible adults capable of making informed decisions about their health. Our online pharmacy offers access to Phenergan for individuals who may have limited availability through traditional pharmacies, prescription‑based insurance schemes, or who are seeking affordable generic alternatives. Always consult your doctor before starting, changing, or discontinuing any medication.

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