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 = 1 January 2014 }}</ref>:


*:[[Pancreatitis]]
*:[[Pancreatitis]]


*: Lactic acidosis/severe hepatomegaly with steatosis  
*: Lactic acidosis/severe hepatomegaly with steatosis


*: Hepatic toxicity  
*: Hepatic toxicity


*: Non-cirrhotic portal hypertension  
*: Non-cirrhotic portal hypertension.


*: [[Peripheral neuropathy]]  
*: [[Peripheral neuropathy]].


*: Retinal changes and [[optic neuritist]]
*: Retinal changes and [[optic neuritist]].


==References==
==References==

Revision as of 20:26, 1 January 2014


Didanosine
VIDEX® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
How Supplied
Labels and Packages

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
  • Hepatic toxicity
  • Non-cirrhotic portal hypertension.

References

  1. "VIDEX (DIDANOSINE) POWDER, FOR SOLUTION [BRISTOL-MYERS SQUIBB COMPANY]". Retrieved 1 January 2014.

Adapted from the FDA Package Insert.