1,393 reports of this reaction
2.8% of all CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE reports
#4 most reported adverse reaction
NAUSEA is the #4 most commonly reported adverse reaction for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, manufactured by Sandoz Inc. There are 1,393 FDA adverse event reports linking CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE to NAUSEA. This represents approximately 2.8% of all 49,809 adverse event reports for this drug.
Patients taking CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE 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 a less commonly reported adverse event for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 1,393 FDA reports for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.8% of all adverse event reports for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE, making it a notable side effect.
If you experience nausea 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.