Nhà máy Stada
Analgesics & Antipyretics

Partamol 325


Pack size:

Box of 1 bottle of 200 tablets.



Each tablet contains paracetamol 325 mg.



48 months from the date of manufacturing.

Store in a well-closed container, in a dry place. Do not store above 30oC.


  • Indications and Dosage & Administration
  • Contraindications
  • Adverse reactions
  • Precautions

  • 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.
  • Partamol 325 is administered orally.
  • For analgesia or antipyrexia in adults or children older than 11 years, the usual oral of paracetamol is 325 - 650 mg every 4 - 6 hours as necessary, but should not exceed 4 g daily; higher single doses (e.g. 1 g) may be useful for analgesia in some patients.
  • Paracetamol should not be used for self-medication of pain for longer than 10 days in adults or 5 days in children.
  • Paracetamol should not be used for self-medication of marker fever (greater than 39.5oC), fever persisting longer 3 days, or recurrent fever.

Or as advised by physicians.


  • Patients with anemia or cardiac, pulmonary, renal, or hepatic disease.
  • Patients with alcohol dependence.
  • Patients with known hypersensitivity to paracetamol or to any ingredient of the drug.
  • Patients with known glucose - 6 - phosphate dehydrogenase deficiency.

  • Skin rash and other allergic reactions occur occasionally. The rash is usually erythematosus or urticarial, but sometimes it is more serious and may be accompanied by drug fever and mucosal lesions.


  • Rash.
  • Nausea, vomiting.
  • Blood dyscrasias (neutropenia, pancytopenia, leukopenia), anemia.
  • Nephropathy, nephrotoxicity with chronic abuse.


  • Hypersensitivity reactions.


  • Paracetamol is relatively nontoxic in therapeutic doses. Dermatologic have sometimes reactions including pruritic maculopapular rash and urticaria; other sensitivity reactions including laryngeal edema, angioedema, and anaphylactoid reactions may occur rarely. Thrombocytopenia, leukopenia, and pancytopenia have been associated with the use of p-aminophenol derivatives, especially with prolonged administration of large doses. Neutropenia and thrombocytopenic purpura have been reported with paracetamol use. Rarely, agranulocytosis has been reported in patients receiving paracetamol.
  • Paracetamol should be used with caution in patients with preexisting anemia, since cyanosis may not be apparent despite dangerously high blood concentrations ofmethemoglobin.
  • 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.
  • 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).
  • Pregnancy: Paracetamol is generally considered to be the analgesic ofchoice in pregnant patients. However, the frequent use of paracetamol in late pregnancy may be associated with an increased risk of persistent wheezing in the infant. Infrequent paracetamol should remain the analgesic ofchoice in pregnancy.
  • Lactation: No adverse effects have been seen in breast-fed infants whose mothers were receiving paracetamol, the amount of paracetamol distributed into breast milk is too small to be harmful to a breast-fed infant.
  • Effects on ability to drive and use machines: None.


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Email : stada@stada.com.vn
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