1,159 reports of this reaction
6.1% of all MISOPROSTOL reports
#2 most reported adverse reaction
ABORTION INCOMPLETE is the #2 most commonly reported adverse reaction for MISOPROSTOL, manufactured by Pfizer Laboratories Div Pfizer Inc. There are 1,159 FDA adverse event reports linking MISOPROSTOL to ABORTION INCOMPLETE. This represents approximately 6.1% of all 18,857 adverse event reports for this drug.
Patients taking MISOPROSTOL who experience abortion incomplete should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABORTION INCOMPLETE is moderately reported among MISOPROSTOL users, representing a notable but not dominant share of adverse events.
In addition to abortion incomplete, the following adverse reactions have been reported for MISOPROSTOL:
ABORTION INCOMPLETE has been reported as an adverse event in 1,159 FDA reports for MISOPROSTOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABORTION INCOMPLETE accounts for approximately 6.1% of all adverse event reports for MISOPROSTOL, making it one of the most commonly reported side effect.
If you experience abortion incomplete while taking MISOPROSTOL, 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.