391 reports of this reaction
3.7% of all TIGECYCLINE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for TIGECYCLINE, manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. There are 391 FDA adverse event reports linking TIGECYCLINE to NAUSEA. This represents approximately 3.7% of all 10,584 adverse event reports for this drug.
Patients taking TIGECYCLINE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among TIGECYCLINE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for TIGECYCLINE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 391 FDA reports for TIGECYCLINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.7% of all adverse event reports for TIGECYCLINE, making it one of the most commonly reported side effect.
If you experience nausea while taking TIGECYCLINE, 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.