402 reports of this reaction
2.6% of all TRIAZOLAM reports
#3 most reported adverse reaction
SOPOR is the #3 most commonly reported adverse reaction for TRIAZOLAM, manufactured by Pharmacia & Upjohn Company LLC. There are 402 FDA adverse event reports linking TRIAZOLAM to SOPOR. This represents approximately 2.6% of all 15,429 adverse event reports for this drug.
Patients taking TRIAZOLAM who experience sopor should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SOPOR is a less commonly reported adverse event for TRIAZOLAM, but still significant enough to appear in the safety profile.
In addition to sopor, the following adverse reactions have been reported for TRIAZOLAM:
SOPOR has been reported as an adverse event in 402 FDA reports for TRIAZOLAM. This does not prove causation, but indicates an association observed in post-market surveillance data.
SOPOR accounts for approximately 2.6% of all adverse event reports for TRIAZOLAM, making it one of the most commonly reported side effect.
If you experience sopor while taking TRIAZOLAM, 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.