CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE

N/A

Manufactured by Sandoz Inc

49,809 FDA adverse event reports analyzed

Last updated: 2026-04-14

About CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE

CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Sandoz Inc. The most commonly reported adverse reactions for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE include DRUG HYPERSENSITIVITY, PAIN, NEUROPATHY PERIPHERAL, NAUSEA, DIARRHOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE.

Top Adverse Reactions

DRUG HYPERSENSITIVITY2,469 reports
PAIN1,589 reports
NEUROPATHY PERIPHERAL1,438 reports
NAUSEA1,393 reports
DIARRHOEA1,379 reports
ARTHRALGIA1,361 reports
FATIGUE1,310 reports
URINARY TRACT INFECTION1,011 reports
PAIN IN EXTREMITY978 reports
DYSPNOEA973 reports
HEADACHE970 reports
DRUG INEFFECTIVE915 reports
ANXIETY899 reports
ASTHENIA884 reports
DIZZINESS852 reports
RASH803 reports
OFF LABEL USE790 reports
VOMITING756 reports
PYREXIA740 reports
ABDOMINAL PAIN717 reports
MALAISE710 reports
WEIGHT DECREASED608 reports
DEPRESSION589 reports
HYPOAESTHESIA586 reports
BACK PAIN581 reports
INSOMNIA575 reports
PNEUMONIA573 reports
PARAESTHESIA550 reports
COUGH533 reports
RENAL FAILURE520 reports
GAIT DISTURBANCE514 reports
PRURITUS504 reports
DEATH503 reports
CHRONIC KIDNEY DISEASE501 reports
FALL489 reports
ABDOMINAL PAIN UPPER480 reports
MYALGIA464 reports
TENDONITIS451 reports
HYPERTENSION446 reports
ACUTE KIDNEY INJURY443 reports
CONDITION AGGRAVATED439 reports
FEELING ABNORMAL430 reports
INJURY413 reports
DEHYDRATION411 reports
CONSTIPATION406 reports
CHEST PAIN402 reports
DECREASED APPETITE399 reports
MUSCLE SPASMS398 reports
HYPERSENSITIVITY390 reports
TENDON RUPTURE378 reports
ABDOMINAL DISCOMFORT375 reports
MUSCULAR WEAKNESS371 reports
CONFUSIONAL STATE360 reports
INFECTION348 reports
URTICARIA344 reports
ANAEMIA339 reports
SINUSITIS329 reports
EMOTIONAL DISTRESS328 reports
HYPOTENSION324 reports
TENDON PAIN315 reports
WEIGHT INCREASED315 reports
TREMOR307 reports
BURNING SENSATION299 reports
OEDEMA PERIPHERAL298 reports
PERIPHERAL SWELLING296 reports
TENDON DISORDER284 reports
JOINT SWELLING279 reports
VISION BLURRED270 reports
CHILLS269 reports
BLOOD PRESSURE INCREASED267 reports
SEPSIS266 reports
PALPITATIONS265 reports
NASOPHARYNGITIS260 reports
ERYTHEMA257 reports
CYSTITIS252 reports
CROHN^S DISEASE246 reports
DRUG INTERACTION242 reports
TINNITUS237 reports
HAEMOGLOBIN DECREASED236 reports
MUSCULOSKELETAL PAIN235 reports
CARDIAC FAILURE CONGESTIVE234 reports
PRODUCT USE ISSUE232 reports
GASTROINTESTINAL DISORDER225 reports
ALOPECIA224 reports
BRONCHITIS220 reports
ABDOMINAL DISTENSION219 reports
GASTROOESOPHAGEAL REFLUX DISEASE215 reports
MEMORY IMPAIRMENT215 reports
MYOCARDIAL INFARCTION210 reports
BALANCE DISORDER204 reports
DYSPEPSIA200 reports
DIVERTICULITIS195 reports
HYPERHIDROSIS192 reports
NERVOUS SYSTEM DISORDER188 reports
DRUG INTOLERANCE187 reports
CEREBROVASCULAR ACCIDENT186 reports
CONTUSION186 reports
CHEST DISCOMFORT185 reports
HALLUCINATION183 reports
MIGRAINE183 reports

Report Outcomes

Out of 20,505 classified reports for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE:

Serious 65.4%Non-Serious 34.6%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female12,413 (66.1%)
Male6,318 (33.7%)
Unknown42 (0.2%)

Reports by Age

Age 65309 reports
Age 63294 reports
Age 67285 reports
Age 66272 reports
Age 61271 reports
Age 57268 reports
Age 60268 reports
Age 64266 reports
Age 68264 reports
Age 69264 reports
Age 62260 reports
Age 56258 reports
Age 70249 reports
Age 71244 reports
Age 59238 reports
Age 58232 reports
Age 53225 reports
Age 72221 reports
Age 55217 reports
Age 50216 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE?

This profile reflects 49,809 FDA FAERS reports that mention CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE?

Frequently reported terms in FAERS include DRUG HYPERSENSITIVITY, PAIN, NEUROPATHY PERIPHERAL, NAUSEA, DIARRHOEA, ARTHRALGIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE?

Labeling and FAERS entries often list Sandoz Inc in connection with CIPROFLOXACIN HYDROCHLORIDE AND HYDROCORTISONE. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.