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LETAIRIS Adverse Event: Gastrooesophageal reflux disease

LETAIRIS Adverse Event: Gastrooesophageal reflux disease is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: LETAIRIS; Product category: Drug; Primary reaction: Gastrooesophageal reflux disease.

Primary drugLETAIRIS
Product categoryDrug
Primary reactionGastrooesophageal reflux disease
All reactionsGastrooesophageal reflux disease
SeriousnessNot serious
Patient outcomeUnknown
Patient sexMale
All drugs reportedLETAIRIS; REVATIO
Reporter countryUS
Reporter type5
Report date20140313
Report ID10007645

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