MESNA INJECTION

N/A

Manufactured by Gland Pharma Limited

16,183 FDA adverse event reports analyzed

Last updated: 2026-04-14

About MESNA INJECTION

MESNA INJECTION is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Gland Pharma Limited. The most commonly reported adverse reactions for MESNA INJECTION include FEBRILE NEUTROPENIA, PYREXIA, OFF LABEL USE, NEUTROPENIA, THROMBOCYTOPENIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for MESNA INJECTION.

Top Adverse Reactions

FEBRILE NEUTROPENIA1,238 reports
PYREXIA667 reports
OFF LABEL USE632 reports
NEUTROPENIA558 reports
THROMBOCYTOPENIA379 reports
ANAEMIA368 reports
VOMITING365 reports
SEPSIS351 reports
NAUSEA350 reports
PANCYTOPENIA342 reports
MUCOSAL INFLAMMATION337 reports
DIARRHOEA335 reports
DISEASE PROGRESSION274 reports
PNEUMONIA274 reports
DEATH249 reports
ENCEPHALOPATHY241 reports
HYPOTENSION219 reports
PLATELET COUNT DECREASED216 reports
DRUG INEFFECTIVE212 reports
PRODUCT USE IN UNAPPROVED INDICATION209 reports
ACUTE KIDNEY INJURY195 reports
INFECTION194 reports
WHITE BLOOD CELL COUNT DECREASED194 reports
LEUKOPENIA193 reports
FATIGUE176 reports
NEUTROPHIL COUNT DECREASED171 reports
DYSPNOEA166 reports
SEPTIC SHOCK165 reports
CYTOKINE RELEASE SYNDROME161 reports
PAIN151 reports
HEADACHE148 reports
CONFUSIONAL STATE147 reports
HYPOKALAEMIA147 reports
TOXICITY TO VARIOUS AGENTS145 reports
BACTERIAL INFECTION142 reports
MYELOSUPPRESSION141 reports
CYSTITIS HAEMORRHAGIC139 reports
STOMATITIS134 reports
NEUROTOXICITY133 reports
ABDOMINAL PAIN126 reports
HYPERTENSION126 reports
HAEMOGLOBIN DECREASED122 reports
DECREASED APPETITE121 reports
PLEURAL EFFUSION120 reports
TACHYCARDIA120 reports
DRUG INTERACTION119 reports
CHILLS114 reports
GENERAL PHYSICAL HEALTH DETERIORATION114 reports
RENAL FAILURE113 reports
BRONCHOPULMONARY ASPERGILLOSIS111 reports
APLASTIC ANAEMIA110 reports
ASTHENIA107 reports
RESPIRATORY FAILURE105 reports
VIRAL INFECTION105 reports
NEUROPATHY PERIPHERAL104 reports
BACK PAIN103 reports
PSEUDOMONAL SEPSIS101 reports
RASH97 reports
MALIGNANT NEOPLASM PROGRESSION96 reports
CONSTIPATION95 reports
MYELODYSPLASTIC SYNDROME95 reports
FUNGAL INFECTION94 reports
CELLULITIS92 reports
CLOSTRIDIUM DIFFICILE COLITIS90 reports
DEHYDRATION90 reports
ALANINE AMINOTRANSFERASE INCREASED88 reports
MALAISE88 reports
HAEMATURIA86 reports
MULTIPLE ORGAN DYSFUNCTION SYNDROME85 reports
SECONDARY IMMUNODEFICIENCY83 reports
ATRIAL FIBRILLATION81 reports
HAEMATOTOXICITY81 reports
CYTOMEGALOVIRUS VIRAEMIA78 reports
CARDIAC ARREST77 reports
CYTOPENIA77 reports
DIZZINESS76 reports
HYPOXIA76 reports
BONE MARROW FAILURE75 reports
COUGH75 reports
PRODUCT USE ISSUE75 reports
URINARY TRACT INFECTION75 reports
HYPONATRAEMIA74 reports
RENAL FAILURE ACUTE73 reports
WEIGHT DECREASED73 reports
BACTERAEMIA72 reports
VENOOCCLUSIVE LIVER DISEASE72 reports
ALOPECIA68 reports
ASPARTATE AMINOTRANSFERASE INCREASED68 reports
EPISTAXIS68 reports
NEUTROPENIC SEPSIS68 reports
RESPIRATORY DISTRESS68 reports
THERAPY NON RESPONDER66 reports
CYTOMEGALOVIRUS INFECTION64 reports
COLITIS62 reports
MENTAL STATUS CHANGES61 reports
PULMONARY EMBOLISM61 reports
VENOOCCLUSIVE DISEASE61 reports
AGRANULOCYTOSIS60 reports
C REACTIVE PROTEIN INCREASED60 reports
HAEMORRHOIDS60 reports

Report Outcomes

Out of 7,956 classified reports for MESNA INJECTION:

Serious 97.4%Non-Serious 2.6%

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

Male3,318 (51.9%)
Female2,903 (45.4%)
Unknown171 (2.7%)

Reports by Age

Age 16162 reports
Age 61143 reports
Age 3132 reports
Age 15129 reports
Age 67125 reports
Age 14111 reports
Age 55111 reports
Age 59111 reports
Age 64109 reports
Age 69107 reports
Age 20102 reports
Age 13101 reports
Age 60100 reports
Age 1095 reports
Age 294 reports
Age 893 reports
Age 6693 reports
Age 792 reports
Age 5792 reports
Age 5892 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 MESNA INJECTION?

This profile reflects 16,183 FDA FAERS reports that mention MESNA INJECTION. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for MESNA INJECTION?

Frequently reported terms in FAERS include FEBRILE NEUTROPENIA, PYREXIA, OFF LABEL USE, NEUTROPENIA, THROMBOCYTOPENIA, ANAEMIA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures MESNA INJECTION?

Labeling and FAERS entries often list Gland Pharma Limited in connection with MESNA INJECTION. 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.