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Phenergan

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Phenergan (Promethazine) is a phenothiazine used to treat allergy symptoms, motion sickness, and nausea. It works by blocking histamine and changing the actions of chemicals in the brain. It is also used as a sedative to help patients relax before medical procedures or to aid sleep.


Ingredient
Availability
In Stock
Delivery Time
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Promethazine
Reference Brand
Phenergan
Manufacturer
Sanofi
Product Form
Tablet, Elixir, Injection
Regulatory Classification
OTC
Primary Category
Allergy & Motion Sickness
Product Category
Antihistamines for systemic use, Phenothiazine derivatives
Pharmacological Class
First-generation Antihistamine
Manufacturer Description
A versatile medicine used for allergies, travel sickness, and as a short-term sedative.
Mechanism of Action
Promethazine is a phenothiazine derivative that works by blocking H1 histamine receptors and exerting significant sedative, anti-motion sickness, and anti-nausea effects through its action on the central nervous system.
Route of Administration
Oral
Onset Time
20 minutes
Duration
4-12 hours
Contraindications
Children under 2 years, Comatose states, Severe CNS depression
Severe Adverse Events
Respiratory depression, Neuroleptic malignant syndrome, Extrapyramidal symptoms, Jaundice
Common Side Effects
Drowsiness, Dry mouth, Blurred vision
Uncommon Side Effects
Dizziness, Confusion, Disorientation, Sensitivity to sunlight
Drug Interactions
Alcohol, Opioids, MAOIs, Anticholinergics
Pregnancy Safety Warnings
Consult a doctor; avoid in the weeks before delivery.
Age Restrictions
Strictly not for children under 2 years
Storage Guidelines
Protect from light and store in a dry place.
Related Products
Cyclizine, Diphenhydramine, Chlorphenamine

Phenergan FAQ

Can Phenergan be used for motion sickness?

Yes, promethazine is sometimes prescribed off-label for motion-induced nausea, but this use is not formally approved in the UK. A prescriber will weigh the benefits against potential side effects such as drowsiness.

Will Phenergan affect my ability to drive?

Phenergan commonly causes drowsiness and can impair reaction time. Avoid driving or operating machinery until you know how the medication affects you, especially after the first dose.

What do the imprints on Phenergan tablets look like?

The 10 mg tablet typically bears the imprint “PH 10” and the 25 mg tablet may show “PH 25”. Imprints can vary between manufacturers; verify with your pharmacist if in doubt.

Is it safe to take Phenergan with antihistamine eye drops?

Concurrent use of multiple antihistamines can increase anticholinergic and sedative effects. Discuss with a healthcare professional before combining them.

Can pregnant women take Phenergan?

Promethazine crosses the placenta and is excreted in breast milk. It should be used during pregnancy only when clearly needed and after a risk-benefit discussion with a prescriber.

How long does the sedative effect of Phenergan last?

Sedation typically peaks within 1-2 hours after ingestion and may persist for 4-6 hours, depending on the dose and individual metabolism.

Will Phenergan interact with my antidepressant medication?

If you are taking a monoamine oxidase inhibitor (MAOI) or a drug that prolongs the QT interval, promethazine may increase the risk of adverse cardiac events. Inform your prescriber of all current medications.

What should I do if I miss a dose before bedtime?

If a dose is missed close to bedtime, it is usually better to skip it and resume the regular schedule the next day. Do not double the dose to “catch up”.

Are there any dietary restrictions while taking Phenergan?

There are no specific food restrictions, but avoid alcohol as it can intensify drowsiness and respiratory depression.

How is Phenergan disposed of if I have leftover tablets?

Unused tablets should be returned to a pharmacy collection point or disposed of according to NHS medication waste guidelines to protect the environment and prevent accidental ingestion.

What is Phenergan?

Phenergan is a brand-name medication that contains promethazine as its active ingredient. The drug is supplied as a pill in strengths of 10 mg and 25 mg. In the United Kingdom Phenergan is classified as a prescription-only medicine (POM) and is marketed by Janssen-Cilag under the supervision of the Medicines and Healthcare products Regulatory Agency (MHRA). Promethazine belongs to the allergy-relief therapeutic class and is also used for nausea, vomiting, and short-term sedation.

How Phenergan Works in the Body

Promethazine is a first-generation antihistamine that works by blocking the H₁ histamine receptors in the central nervous system and peripheral tissues. By inhibiting these receptors, it reduces the effects of histamine-one of the primary mediators of allergic symptoms such as itching, sneezing, and runny nose.

In addition to its antihistamine activity, promethazine has anticholinergic and sedative properties. The anticholinergic effect contributes to drying of secretions, which can be helpful in treating motion-related nausea, while the sedative action results from central nervous system depression and is useful for pre-operative anxiety or short-term sleep aid.

Conditions Treated by Phenergan

  • Allergic rhinitis and urticaria - relief of itching, sneezing, and hives.
  • Nausea and vomiting - useful in postoperative settings, chemotherapy-induced nausea, and motion sickness.
  • Sedation - short-term use before surgery or for severe insomnia when advised by a clinician.

These indications are approved by the MHRA for the UK market. The drug is generally prescribed for adults and for children older than two years when the benefit outweighs the risk.

Evidence-Based Off-Label Uses

Promethazine has been studied for a few off-label purposes, such as treatment of anxiety in the short term and as an adjunct in migraine therapy. These uses are not approved by the MHRA and should only be considered under close medical supervision with an individualized risk assessment.

Who Should (Not) Use Phenergan?

Absolute contraindications

  • Known hypersensitivity to promethazine or any other antihistamine.
  • Use in newborns and infants younger than 2 years (risk of severe respiratory depression).
  • Patients in a state of deep coma, severe central nervous system depression, or untreated narrow-angle glaucoma.

Relative contraindications

  • Severe hepatic or renal impairment - dose adjustment may be required.
  • Pregnancy and lactation - promethazine crosses the placenta and is excreted in breast milk; it should be used only if clearly needed and after risk-benefit discussion.
  • Elderly patients - increased sensitivity to sedative and anticholinergic effects; start at the lowest effective dose.

If you have any of these conditions, discuss alternative treatments with your healthcare provider.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Drowsiness or sedation - reported in the majority of patients.
  • Dry mouth, blurred vision, and constipation (anticholinergic effects).
  • Dizziness or light-headedness, especially when standing quickly.

These effects are generally mild and transient. Drinking plenty of water and avoiding sudden position changes can help.

Serious Adverse Events

  • Respiratory depression, particularly in very young children or when combined with other depressants.
  • Extrapyramidal symptoms (e.g., tremor, rigidity) - rare but require immediate medical attention.
  • Severe allergic reactions such as rash, swelling, or anaphylaxis.
  • Cardiac arrhythmias related to QT-interval prolongation; monitor closely if you have existing heart disease.

Drug Interactions

  • Central nervous system depressants (opioids, benzodiazepines, barbiturates, alcohol) - may enhance sedation and respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs) - can increase anticholinergic toxicity; a wash-out period of at least 14 days is recommended.
  • Other antihistamines - additive anticholinergic and sedative effects.
  • Drugs that prolong the QT interval (e.g., certain antiarrhythmics, fluoroquinolone antibiotics) - increase the risk of cardiac arrhythmias.

Food and Lifestyle Interactions

  • Alcohol - amplifies drowsiness and respiratory depression; avoid or limit intake.
  • Operating heavy machinery or driving should be avoided until you know how Phenergan affects you.

If you are taking other medicines, herbal supplements, or over-the-counter products, inform your pharmacist or prescriber before starting Phenergan.

How to Take Phenergan

  • Standard adult dosing for allergy relief:

  • 10 mg tablet: one tablet every 4-6 hours as needed.

  • 25 mg tablet: one tablet every 6-8 hours as needed.

  • Do not exceed 100 mg per day without medical advice.

  • Special populations:

  • Elderly: start with the lowest effective dose (usually 10 mg) and assess tolerance.

  • Renal or hepatic impairment: dose may need reduction; follow prescriber guidance.

  • Children (≥2 years): dosing is weight-based, typically 0.5 mg/kg per dose, not exceeding adult maximum.

  • Administration: Swallow the tablet whole with a full glass of water. It may be taken with or without food; food can slightly delay absorption but does not alter effectiveness.

  • Missed dose: If you remember a missed dose and it is more than 4 hours since the scheduled time, take it now. If the next dose is due within a short interval, skip the missed dose-do not double-dose.

  • Overdose: Symptoms may include extreme drowsiness, confusion, fever, rapid heartbeat, and seizures. Call emergency services (999 in the UK) and provide the tablet strength(s) taken. Treatment is supportive; activated charcoal may be used, and physostigmine is an antidote for severe anticholinergic toxicity under medical supervision.

  • Discontinuation: Phenergan does not normally require tapering. However, abrupt cessation after prolonged high-dose use may cause rebound insomnia or agitation; discuss any planned discontinuation with your prescriber.

Monitoring and Follow-Up

  • Clinical monitoring: Observe for excessive sedation, respiratory difficulty, or signs of allergic reaction after the first few doses.
  • Laboratory tests: Generally not required for short-term use. For chronic therapy, periodic liver function tests may be advisable in patients with hepatic disease.

Regular follow-up with a healthcare professional ensures the medication remains appropriate and safe.

Storage and Handling

  • Store tablets at room temperature (15-30 °C), away from excess moisture and direct sunlight.
  • Keep the medication out of reach of children and pets.
  • Do not use tablets after the expiry date printed on the pack.
  • Dispose of unused tablets according to local pharmacy-take-back schemes or NHS guidelines for medication waste.

Medication-Specific Glossary

Antihistamine
A drug that blocks histamine H₁ receptors, reducing allergic symptoms such as itching, swelling, and redness.
Anticholinergic
A property that inhibits the action of acetylcholine on muscarinic receptors, leading to effects like dry mouth, blurred vision, and reduced secretions.
QT-interval prolongation
Lengthening of the heart’s electrical repolarisation period on an ECG, which can increase the risk of a potentially life-threatening arrhythmia called torsades de pointes.
Sedation
A state of calmness, drowsiness, or reduced alertness induced by a medication’s central nervous system depressant effects.

Medical Disclaimer

This article provides educational information about Phenergan and is not a substitute for professional medical advice. Treatment decisions, including the use of unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Information for Phenergan is sourced from established medical standards and updated frequently. It is provided for general guidance and should be confirmed with a healthcare professional before use.
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