PURIFIED WATER

N/A

Manufactured by McKesson

130 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PURIFIED WATER

PURIFIED WATER is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by McKesson. The most commonly reported adverse reactions for PURIFIED WATER include EYE IRRITATION, DRUG HYPERSENSITIVITY, EYE PAIN, INTERSTITIAL LUNG DISEASE, NAUSEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PURIFIED WATER.

Top Adverse Reactions

EYE IRRITATION5 reports
DRUG HYPERSENSITIVITY3 reports
EYE PAIN3 reports
INTERSTITIAL LUNG DISEASE3 reports
NAUSEA3 reports
OESOPHAGITIS3 reports
OFF LABEL USE3 reports
THROMBOCYTOPENIA3 reports
COUGH2 reports
DEPRESSED MOOD2 reports
EYE PRURITUS2 reports
EYE SWELLING2 reports
FATIGUE2 reports
HEADACHE2 reports
LACRIMATION INCREASED2 reports
MALAISE2 reports
OCULAR HYPERAEMIA2 reports
PAIN2 reports
PAIN IN EXTREMITY2 reports
VOMITING2 reports
ABDOMINAL ABSCESS1 reports
ABDOMINAL PAIN1 reports
ABSCESS1 reports
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER1 reports
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN1 reports
ADRENAL INSUFFICIENCY1 reports
AFFECT LABILITY1 reports
AGRANULOCYTOSIS1 reports
ANAEMIA1 reports
ANAPHYLACTIC REACTION1 reports
ANHEDONIA1 reports
ANXIETY1 reports
ARTHRALGIA1 reports
ASTHENIA1 reports
BACK PAIN1 reports
BLOOD PARATHYROID HORMONE INCREASED1 reports
BLOOD PRESSURE INCREASED1 reports
CANDIDA INFECTION1 reports
CANDIDA TEST POSITIVE1 reports
CHOLESTASIS1 reports
COLONY STIMULATING FACTOR THERAPY1 reports
DEATH1 reports
DEPRESSION1 reports
DEVICE USE ISSUE1 reports
DIARRHOEA1 reports
DRUG ABUSE1 reports
DRUG DEPENDENCE1 reports
DRUG INEFFECTIVE1 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION1 reports
DRUG WITHDRAWAL SYNDROME1 reports
DYSGEUSIA1 reports
DYSPHONIA1 reports
DYSPNOEA1 reports
EMOTIONAL DISTRESS1 reports
ENTEROCOCCAL INFECTION1 reports
ENTEROCOLITIS1 reports
EOSINOPHILIC PNEUMONIA1 reports
EPICONDYLITIS1 reports
EXOPHTHALMOS1 reports
EYE CONTUSION1 reports
EYE DISCHARGE1 reports
EYELID EXFOLIATION1 reports
EYELID MARGIN CRUSTING1 reports
FACIAL PAIN1 reports
FACIAL PALSY1 reports
FEBRILE NEUTROPENIA1 reports
FEELING OF BODY TEMPERATURE CHANGE1 reports
FISTULA1 reports
FLUSHING1 reports
FUNGAL INFECTION1 reports
GAIT DISTURBANCE1 reports
GENERAL PHYSICAL HEALTH DETERIORATION1 reports
GINGIVAL BLEEDING1 reports
GRAFT VERSUS HOST DISEASE1 reports
HAEMOLYTIC ANAEMIA1 reports
HEPATIC CYTOLYSIS1 reports
HEPATIC FUNCTION ABNORMAL1 reports
HERPES OPHTHALMIC1 reports
HOSPITALISATION1 reports
HYPERTHERMIA1 reports
HYPOGLYCAEMIC COMA1 reports
IDIOPATHIC PULMONARY FIBROSIS1 reports
INCORRECT ROUTE OF DRUG ADMINISTRATION1 reports
INJECTION SITE BRUISING1 reports
INJECTION SITE MASS1 reports
INJECTION SITE PAIN1 reports
INTESTINAL PERFORATION1 reports
IRRITABILITY1 reports
LOSS OF CONSCIOUSNESS1 reports
LUNG CYST1 reports
MEMORY IMPAIRMENT1 reports
MOOD SWINGS1 reports
MUSCULOSKELETAL PAIN1 reports
MYALGIA1 reports
NASAL CONGESTION1 reports
NEOPLASM PROGRESSION1 reports
NEURALGIA1 reports
NEUTROPENIA1 reports
NEUTROPHIL COUNT DECREASED1 reports
OSTEOPOROSIS1 reports

Report Outcomes

Out of 47 classified reports for PURIFIED WATER:

Serious 72.3%Non-Serious 27.7%

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

Female25 (58.1%)
Male18 (41.9%)

Reports by Age

Age 292 reports
Age 522 reports
Age 532 reports
Age 632 reports
Age 722 reports
Age 732 reports
Age 782 reports
Age 141 reports
Age 161 reports
Age 211 reports
Age 411 reports
Age 451 reports
Age 491 reports
Age 571 reports
Age 581 reports
Age 601 reports
Age 611 reports
Age 621 reports
Age 651 reports
Age 701 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 PURIFIED WATER?

This profile reflects 130 FDA FAERS reports that mention PURIFIED WATER. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PURIFIED WATER?

Frequently reported terms in FAERS include EYE IRRITATION, DRUG HYPERSENSITIVITY, EYE PAIN, INTERSTITIAL LUNG DISEASE, NAUSEA, OESOPHAGITIS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PURIFIED WATER?

Labeling and FAERS entries often list McKesson in connection with PURIFIED WATER. 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.