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6.0

Adverse Drug Reactions (ADRS)

Malawi Standard Treatment Guidelines, 6th Edition, 2023. Chapter 0, Prescribing Guidelines.

Clinical Description

  • Nearly all medicines may produce unwanted or unexpected adverse effects, some of which may be life threatening e.g., anaphylactic shock, liver failure
  • Prescribers should immediately report any serious or unexpected adverse effects thought to be due to a medicine to:

The Registrar, Pharmacy and Medicines Regulatory Authority, PO Box 30241, Lilongwe.

Tel: 01 755 165/166 Fax: 01755 204

  • Ways to minimize ADRs

Never use a medicine unless there is a clear indication for its use

  • Only use medicines in pregnancy if essential
  • Check if the patient has had any previous reactions to the medicine or to similar medicines
  • Remember to reduce doses when necessary e.g., in the young, the elderly, and if liver or renal disease is present
  • Always prescribe the minimum number of medicines possible.
  • Carefully explain the dose regimens to patients, especially those on multiple medicines, the elderly and anyone likely to misunderstand.
  • If possible, use medicines with which you are familiar
  • look out for ADRs when using new or unfamiliar medicines
  • Warn patients about likely adverse effects and advise them on what to do if they occur
  • Patients on certain prolonged treatments e.g., Anticoagulants, corticosteroids, Insulin etc. should carry a health passport giving information about the treatment

Check doses against the printed guideline and your clinical judgement before treating a patient. Spotted an error? Report it from the contact links below.

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