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Diphtheria

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Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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Anthelminthic Agents

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Related Experiment Video

Updated: May 26, 2026

Optimized Griess Reaction for UV-Vis and Naked-eye Determination of Anti-malarial Primaquine
08:31

Optimized Griess Reaction for UV-Vis and Naked-eye Determination of Anti-malarial Primaquine

Published on: October 11, 2019

Case report: Peripheral polyneuropathy and mefloquine prophylaxis.

Alexander C Chester1, Paola Sandroni

  • 1Department of Medicine, Georgetown University Hospital, Washington, DC 20016, USA. achester@foxhallinternists.com

The American Journal of Tropical Medicine and Hygiene
|December 7, 2011
PubMed
Summary

A woman developed peripheral polyneuropathy after taking mefloquine hydrochloride for malaria prevention. This rare adverse effect, affecting peripheral nerves, is seldom documented following mefloquine use.

Related Experiment Videos

Last Updated: May 26, 2026

Optimized Griess Reaction for UV-Vis and Naked-eye Determination of Anti-malarial Primaquine
08:31

Optimized Griess Reaction for UV-Vis and Naked-eye Determination of Anti-malarial Primaquine

Published on: October 11, 2019

Area of Science:

  • Neuroscience
  • Pharmacology
  • Tropical Medicine

Background:

  • Mefloquine hydrochloride is a common antimalarial drug.
  • Central nervous system side effects of mefloquine are well-documented.
  • Peripheral neuropathy is a less common but serious adverse event.

Observation:

  • A case of peripheral polyneuropathy is presented in a woman after completing malaria prophylaxis with mefloquine hydrochloride.
  • The patient received 4 weekly doses of 250 mg mefloquine hydrochloride.
  • The onset of symptoms occurred shortly after the completion of the prophylactic regimen.

Findings:

  • The presented case highlights a rare instance of peripheral polyneuropathy potentially linked to mefloquine hydrochloride.
  • This specific presentation of peripheral nerve involvement is seldom reported in medical literature.
  • The neurological complication manifested as peripheral polyneuropathy, distinct from more common central nervous system effects.

Implications:

  • This case underscores the importance of considering peripheral polyneuropathy in patients presenting with neurological symptoms after mefloquine use.
  • Further research may be warranted to elucidate the mechanisms underlying mefloquine-induced peripheral polyneuropathy.
  • Clinicians should be vigilant for rare neurological adverse events associated with mefloquine prophylaxis.