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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