199 reports of this reaction
1.6% of all DACARBAZINE reports
#16 most reported adverse reaction
PULMONARY TOXICITY is the #16 most commonly reported adverse reaction for DACARBAZINE, manufactured by Fresenius Kabi USA, LLC. There are 199 FDA adverse event reports linking DACARBAZINE to PULMONARY TOXICITY. This represents approximately 1.6% of all 12,161 adverse event reports for this drug.
Patients taking DACARBAZINE who experience pulmonary toxicity should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PULMONARY TOXICITY is a less commonly reported adverse event for DACARBAZINE, but still significant enough to appear in the safety profile.
In addition to pulmonary toxicity, the following adverse reactions have been reported for DACARBAZINE:
The following drugs have also been linked to pulmonary toxicity in FDA adverse event reports:
PULMONARY TOXICITY has been reported as an adverse event in 199 FDA reports for DACARBAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PULMONARY TOXICITY accounts for approximately 1.6% of all adverse event reports for DACARBAZINE, making it a notable side effect.
If you experience pulmonary toxicity while taking DACARBAZINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.