411 reports of this reaction
1.9% of all PIPERACILLIN AND TAZOBACTAM reports
#10 most reported adverse reaction
SEPTIC SHOCK is the #10 most commonly reported adverse reaction for PIPERACILLIN AND TAZOBACTAM, manufactured by Apotex Corp.. There are 411 FDA adverse event reports linking PIPERACILLIN AND TAZOBACTAM to SEPTIC SHOCK. This represents approximately 1.9% of all 21,987 adverse event reports for this drug.
Patients taking PIPERACILLIN AND TAZOBACTAM who experience septic shock should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SEPTIC SHOCK is a less commonly reported adverse event for PIPERACILLIN AND TAZOBACTAM, but still significant enough to appear in the safety profile.
In addition to septic shock, the following adverse reactions have been reported for PIPERACILLIN AND TAZOBACTAM:
The following drugs have also been linked to septic shock in FDA adverse event reports:
SEPTIC SHOCK has been reported as an adverse event in 411 FDA reports for PIPERACILLIN AND TAZOBACTAM. This does not prove causation, but indicates an association observed in post-market surveillance data.
SEPTIC SHOCK accounts for approximately 1.9% of all adverse event reports for PIPERACILLIN AND TAZOBACTAM, making it a notable side effect.
If you experience septic shock while taking PIPERACILLIN AND TAZOBACTAM, 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.