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INN monograph

Paracetamol / Diphenhydramine

Non-opioid analgesic / antipyretic · POM

POM Source-linked Grade A-

Source-linked · Updated 03 Aug 2026 · Source: Local active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Component monographs (multi-source pipeline)

Kenya market

Wholesale / list prices where loaded

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Brands
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Risk first

Contraindications

  • [Paracetamol] Severe active hepatic disease / acute liver failure.
  • Hypersensitivity.
  • Chronic heavy alcohol use — use reduced maximum daily dose or avoid. [Diphenhydramine] Hypersensitivity to the active substance or excipients.
  • Additional absolute contraindications are indication- and product-specific — consult SmPC.

Precautions

  • [From component Paracetamol] Risk of severe hepatotoxicity in overdose.
  • Chronic high-dose use, malnutrition, enzyme-inducing drugs, and alcohol increase risk.
  • Check total daily intake from all sources.

Point of care

Dosing

Adult

Dosing is indication-, age-, weight- and organ-function-specific for this INN. Do not use class averages for high-risk patients. Confirm the exact regimen in the current SmPC and Kenya Standard Treatment Guidelines. Typical professional workflow: (1) confirm indication, (2) check renal/hepatic function, (3) screen interactions/allergies, (4) select dose/route/duration, (5) define monitoring.

Paediatric

Paediatric dosing is weight- and age-based; use a paediatric formulary / SmPC. Do not extrapolate adult tablets without calculation.

Renal

Generally safe; prolonged high dose rare associations — prefer careful use in advanced CKD.

  • CrCl 0–120: Confirm renal dosing in product SmPC / primary label.

Hepatic

PRIMARY toxicity organ in overdose; therapeutic doses usually safe if daily limits respected.

Safety

Drug interactions

Open checker →
  • First-line for mild–moderate pain and fever.
  • Calculate total daily exposure from all sources.
  • In overdose: timed levels + NAC per protocol — do not wait for symptoms.

Safety

Adverse effects

  • [Paracetamol] Rare at therapeutic doses.
  • Serious: acute liver failure in overdose, rare severe skin reactions (SJS/TEN/AGEP). [Diphenhydramine] Adverse reactions vary by agent.
  • Counsel on common predictable effects and serious warning symptoms (allergy, severe rash, jaundice, unusual bleeding, severe GI symptoms, neurological changes).
  • Report suspected ADRs via national pharmacovigilance channels.

Use

Indications

  • Therapeutic use is agent- and indication-specific within the class (Non-opioid analgesic / antipyretic).
  • Use according to culture results, national guidelines (Kenya STG/EML where applicable) and the current product SmPC.

Pharmacology

Mode of action

Combination product.

Inhibit COX ↓ Prostaglandins Analgesia / anti-inflammatory
Full mechanism text

Combination product. Component mechanism (Paracetamol): Inhibitors of cyclo-oxygenase [COX-1 and COX-2] enzyme that catalyzes the conversion of arachidonic acid to PGH2.

ADME

Pharmacokinetics & PD

Onset 30–60 minutes oral
Duration 4–6 hours
Route ORAL / RECTAL / IV
Metabolism (glucuronidation/sulfation); toxic NAPQI pathway via CYP2E1 when pathways saturated or glutathione depleted.
Half-life ~2–3 h; prolonged in liver disease/overdose.
Full PK/PD text

Rapid oral absorption. Hepatic metabolism (glucuronidation/sulfation); toxic NAPQI pathway via CYP2E1 when pathways saturated or glutathione depleted. Half-life ~2–3 h; prolonged in liver disease/overdose.

Kenya

Brands & prices

0 listed
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No brands linked yet.

Special populations

Pregnancy & lactation

Pregnancy

[Paracetamol] Analgesic/antipyretic of choice in pregnancy when needed; use lowest effective dose/shortest duration. [Diphenhydramine] Use only if potential benefit justifies potential risk; prefer agents with better reproductive data when alternatives exist.

Lactation

Compatible with breastfeeding at standard doses.

Diet

Food & alcohol

  • Food
  • Food

Trust

Sources & disclaimer

Source: Local active-ingredient clinical extract; RxNorm (NLM RxNav); PubChem; Component monographs (multi-source pipeline)

Open source link

Clinical review date not recorded.

Decision support only — not a substitute for clinical judgment, product SmPC, or Kenya STG/EML.

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