1,589 reports of this reaction
3.2% of all CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE reports
#2 most reported adverse reaction
PAIN is the #2 most commonly reported adverse reaction for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, manufactured by Sandoz Inc. There are 1,589 FDA adverse event reports linking CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE to PAIN. This represents approximately 3.2% of all 49,809 adverse event reports for this drug.
Patients taking CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE who experience pain should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PAIN is moderately reported among CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE users, representing a notable but not dominant share of adverse events.
In addition to pain, the following adverse reactions have been reported for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE:
The following drugs have also been linked to pain in FDA adverse event reports:
PAIN has been reported as an adverse event in 1,589 FDA reports for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PAIN accounts for approximately 3.2% of all adverse event reports for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, making it one of the most commonly reported side effect.
If you experience pain while taking CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, 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.