Didanosine adverse reactions: Difference between revisions
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==Adverse Reactions== | ==Adverse Reactions== | ||
The following adverse reactions are discussed in greater detail in other sections: | The following adverse reactions are discussed in greater detail in other sections<ref name="dailymed.nlm.nih.gov">{{Cite web | last = | first = | title = VIDEX (DIDANOSINE) POWDER, FOR SOLUTION [BRISTOL-MYERS SQUIBB COMPANY] | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4401ca0-98ae-af38-84c7-2f615d0706b9#nlm34089-3| publisher = | date = | accessdate = }}</ref>: | ||
* [[Pancreatitis]] | |||
* [[Lactic acidosis]]/severe [[hepatomegaly]] with [[steatosis]] | |||
* [[Hepatotoxicity|Hepatic toxicity]] | |||
* Non-cirrhotic [[portal hypertension]] | |||
* [[Peripheral neuropathy]] | |||
* | * Retinal changes and [[optic neuritis]] | ||
==References== | ==References== | ||
Latest revision as of 05:52, 5 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[1]:
- Lactic acidosis/severe hepatomegaly with steatosis
- Non-cirrhotic portal hypertension
- Retinal changes and optic neuritis
References
Adapted from the FDA Package Insert.