Stavudine adverse reactions: Difference between revisions
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The following adverse reactions are discussed in greater detail in other sections of the labeling: | The following adverse reactions are discussed in greater detail in other sections of the labeling: | ||
*:[[ | *:[[Lactic acidosis]] and severe [[hepatomegaly]] with steatosis | ||
*: | |||
*:Hepatic injury | |||
*:Neurologic symptoms and motor weakness | *:Neurologic symptoms and motor weakness | ||
*:[[Pancreatitis]] | *:[[Pancreatitis]] | ||
*:[[lipoatrophy]]/[[lipodystrophy]] | *:[[lipoatrophy]]/[[lipodystrophy]] | ||
Latest revision as of 07:14, 3 January 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2]
Adverse Reactions
The following adverse reactions are discussed in greater detail in other sections of the labeling:
- Lactic acidosis and severe hepatomegaly with steatosis
- Hepatic injury
- Neurologic symptoms and motor weakness
When ZERIT is used in combination with other agents with similar toxicities, the incidence of adverse reactions may be higher than when stavudine is used alone.[1]
References
Adapted from the FDA Package Insert.