CEFPODOXIME PROXETIL

N/A

Manufactured by Amici Pharmaceuticals, LLC.

1,861 FDA adverse event reports analyzed

Last updated: 2026-04-15

About CEFPODOXIME PROXETIL

CEFPODOXIME PROXETIL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Amici Pharmaceuticals, LLC.. The most commonly reported adverse reactions for CEFPODOXIME PROXETIL include DIARRHOEA, PYREXIA, PNEUMONIA, DYSPNOEA, COUGH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for CEFPODOXIME PROXETIL.

Top Adverse Reactions

DIARRHOEA77 reports
PYREXIA75 reports
PNEUMONIA62 reports
DYSPNOEA46 reports
COUGH43 reports
FATIGUE43 reports
NAUSEA41 reports
VOMITING39 reports
ASTHENIA36 reports
DEATH36 reports
PAIN36 reports
RASH33 reports
HEADACHE32 reports
CONDITION AGGRAVATED31 reports
URINARY TRACT INFECTION31 reports
DIZZINESS29 reports
OFF LABEL USE29 reports
DRUG INEFFECTIVE28 reports
PRURITUS26 reports
ANAEMIA24 reports
DEHYDRATION24 reports
DRUG HYPERSENSITIVITY23 reports
FALL22 reports
WEIGHT DECREASED21 reports
ABDOMINAL PAIN20 reports
BRONCHITIS20 reports
CONSTIPATION20 reports
DECREASED APPETITE20 reports
GENERAL PHYSICAL HEALTH DETERIORATION20 reports
MALAISE19 reports
PLEURAL EFFUSION19 reports
WHITE BLOOD CELL COUNT DECREASED19 reports
ANXIETY18 reports
ERYTHEMA18 reports
RENAL FAILURE18 reports
BLADDER TRANSITIONAL CELL CARCINOMA17 reports
INFECTION17 reports
INSOMNIA17 reports
ACUTE KIDNEY INJURY16 reports
ARTHRALGIA16 reports
HAEMOGLOBIN DECREASED16 reports
NASOPHARYNGITIS16 reports
NEUTROPENIA16 reports
SEPSIS16 reports
STEVENS JOHNSON SYNDROME16 reports
BACK PAIN15 reports
ILLNESS15 reports
OEDEMA PERIPHERAL15 reports
ANGIOEDEMA14 reports
CHILLS14 reports
GAIT DISTURBANCE14 reports
PAIN IN EXTREMITY14 reports
PLATELET COUNT DECREASED14 reports
CLOSTRIDIUM DIFFICILE COLITIS13 reports
RENAL FAILURE ACUTE13 reports
SOMNOLENCE13 reports
THROMBOCYTOPENIA13 reports
ABDOMINAL PAIN UPPER12 reports
CONFUSIONAL STATE12 reports
DRUG INTERACTION12 reports
EOSINOPHILIA12 reports
LUNG DISORDER12 reports
PRODUCT DOSE OMISSION ISSUE12 reports
PULMONARY EMBOLISM12 reports
BALANCE DISORDER11 reports
CHEST PAIN11 reports
FEBRILE NEUTROPENIA11 reports
GASTROINTESTINAL DISORDER11 reports
HYPERTENSION11 reports
INFLUENZA11 reports
PANCREATITIS ACUTE11 reports
TACHYCARDIA11 reports
UPPER RESPIRATORY TRACT INFECTION11 reports
AGRANULOCYTOSIS10 reports
CHEST DISCOMFORT10 reports
COLITIS10 reports
GASTROINTESTINAL HAEMORRHAGE10 reports
HYPOKALAEMIA10 reports
MALIGNANT NEOPLASM PROGRESSION10 reports
PARAESTHESIA10 reports
SINUSITIS10 reports
TOXIC EPIDERMAL NECROLYSIS10 reports
URTICARIA10 reports
VISION BLURRED10 reports
ALANINE AMINOTRANSFERASE INCREASED9 reports
ASTHMA9 reports
BLOOD PRESSURE INCREASED9 reports
DEPRESSION9 reports
DISEASE PROGRESSION9 reports
DYSGEUSIA9 reports
GASTROOESOPHAGEAL REFLUX DISEASE9 reports
HYPOAESTHESIA9 reports
HYPOTENSION9 reports
INFLAMMATION9 reports
PRODUCT USE ISSUE9 reports
PRODUCTIVE COUGH9 reports
ASPARTATE AMINOTRANSFERASE INCREASED8 reports
DYSPHAGIA8 reports
FEELING ABNORMAL8 reports
HYPERHIDROSIS8 reports

Report Outcomes

Out of 915 classified reports for CEFPODOXIME PROXETIL:

Serious 84.2%Non-Serious 15.8%

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

Female498 (57.6%)
Male366 (42.4%)

Reports by Age

Age 6225 reports
Age 7022 reports
Age 7922 reports
Age 7118 reports
Age 6017 reports
Age 7317 reports
Age 6416 reports
Age 5614 reports
Age 6914 reports
Age 5313 reports
Age 5813 reports
Age 7512 reports
Age 7612 reports
Age 7812 reports
Age 2910 reports
Age 6110 reports
Age 6510 reports
Age 6610 reports
Age 8110 reports
Age 249 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 CEFPODOXIME PROXETIL?

This profile reflects 1,861 FDA FAERS reports that mention CEFPODOXIME PROXETIL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for CEFPODOXIME PROXETIL?

Frequently reported terms in FAERS include DIARRHOEA, PYREXIA, PNEUMONIA, DYSPNOEA, COUGH, FATIGUE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures CEFPODOXIME PROXETIL?

Labeling and FAERS entries often list Amici Pharmaceuticals, LLC. in connection with CEFPODOXIME PROXETIL. 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.