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Partamol eff.
OTC

Partamol eff. contains paracetamol. In equal doses, the degree of analgesia and antipyresis produced by paracetamol is similar to that produced by aspirin. Paracetamol lowers body temperature in patients with fever but rarely lowers normal body temperature.

Pack size Box of 4 strips x 4 tablets. Box of 1 tube, 2 tubes x 10 tablets
Shelf-life 36 months
Composition Paracetamol
Dosage forms and strengths Effervescent tablet: 500 mg
Product code :

PRESCRIBING INFORMATION

Indications

  • For treatment of mild to moderate pain and fever, especially in patients in whom salicylates are contraindicated or not tolerated.
  • The drug is most effective in relieving low intensity pain of non-visceral origin.

Dosage

  • Paracetamol should not be used for self-medication of pain for longer than 10 days in adults and 5 days in children.
  • Paracetamol should not be used for self-medication of marked fever (greater than 39.5oC), fever persisting longer than 3 days, or recurrent fever.
  • Adults and children ≥ 11 years of age: 1 tablet every 4 – 6 hours as necessary, not exceed 4 g daily.

Usage

  • Partamol eff. is administered orally. The effervescent tablet is dissolved in a glass of water.
  • Patients with known hypersensitivity to paracetamol or to any of the excipients listed in.
  • Patients with severe hepatic impairment.

Uncommon

  •  Skin rash and other allergic reactions occur occasionally, usually erythematosus or urticaria,
  • Nausea, vomiting,
  • Blood dyscrasias (neutropenia, pancytopenia, leukopenia), anemia,
  • Nephropathy, nephrotoxicity with chronic abuse.
  • Paracetamol should be used with caution in patients with preexisting anemia, since cyanosis may not be apparent despite dangerously high blood concentrations of methemoglobin.
  • Excessive intake of alcohol may increase the risk of paracetamol induced hepatotoxicity; avoid or limit alcohol intake.
  • Caution is recommended when giving to patients with hepatic or renal impairment, susceptible individuals.
  • The physicians need to warn the patients of the signs of serious skin reactions known as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN) or Lyell’s syndrome, acute generalized exanthematous pustulosis (AGEP).
  • Partamol eff. contains aspartame. Aspartame is a source of phenylalanine. It may be harmful if you have phenylketonuria (PKU), a rare genetic disorder in which phenylalanine builds up because the body cannot remove it properly.
  • Partamol eff. contains anhydrous sodium bicarbonate, anhydrous sodium carbonate, sodium benzoate, sodium saccharin; therefore, patients should have dietary sodium restriction.
  • Paracetamol should be only used in pregnant women when clearly needed. Caution when use paracetamol for breastfeeding women.
  • Patients should be aware of how they react to Partamol eff. before driving or operating machinery.