WATER

N/A

9,176 FDA adverse event reports analyzed

Last updated: 2026-04-15

About WATER

WATER is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for WATER include HEREDITARY ANGIOEDEMA, FATIGUE, NAUSEA, HEADACHE, PRODUCT DOSE OMISSION ISSUE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for WATER.

Top Adverse Reactions

HEREDITARY ANGIOEDEMA527 reports
FATIGUE257 reports
NAUSEA255 reports
HEADACHE236 reports
PRODUCT DOSE OMISSION ISSUE230 reports
PAIN208 reports
WEIGHT DECREASED208 reports
WEIGHT INCREASED201 reports
PYREXIA200 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION190 reports
DYSPNOEA189 reports
VOMITING187 reports
DIARRHOEA154 reports
OFF LABEL USE152 reports
COUGH149 reports
COVID 19146 reports
DIZZINESS144 reports
DRUG INEFFECTIVE144 reports
NASOPHARYNGITIS143 reports
SINUSITIS140 reports
NO ADVERSE EVENT137 reports
FALL133 reports
PNEUMONIA133 reports
MALAISE130 reports
MYELOSUPPRESSION123 reports
ARTHRALGIA110 reports
CONDITION AGGRAVATED105 reports
PRODUCT USE ISSUE103 reports
PRURITUS101 reports
DEATH96 reports
PAIN IN EXTREMITY94 reports
RASH93 reports
ILLNESS91 reports
PRODUCT USE IN UNAPPROVED INDICATION89 reports
ABDOMINAL PAIN85 reports
CHILLS85 reports
INJECTION SITE PAIN84 reports
URINARY TRACT INFECTION83 reports
ASTHENIA82 reports
HOSPITALISATION79 reports
INFLUENZA79 reports
ANXIETY75 reports
BACK PAIN73 reports
PRESCRIBED OVERDOSE73 reports
POOR VENOUS ACCESS72 reports
WHITE BLOOD CELL COUNT DECREASED72 reports
CHEST DISCOMFORT71 reports
INFECTION71 reports
MUSCLE SPASMS70 reports
HYPERTENSION69 reports
BLOOD PRESSURE INCREASED68 reports
CHEST PAIN67 reports
INFUSION RELATED REACTION64 reports
INSURANCE ISSUE63 reports
ABDOMINAL DISTENSION62 reports
ERYTHEMA62 reports
HEART RATE INCREASED61 reports
HYPERSENSITIVITY58 reports
INCORRECT DOSE ADMINISTERED56 reports
CONTUSION55 reports
URTICARIA55 reports
PERIPHERAL SWELLING53 reports
PRODUCT PACKAGING QUANTITY ISSUE52 reports
FEELING ABNORMAL51 reports
DEVICE RELATED INFECTION50 reports
UPPER RESPIRATORY TRACT INFECTION50 reports
THROMBOSIS49 reports
ABDOMINAL PAIN UPPER48 reports
DRUG HYPERSENSITIVITY48 reports
BURNING SENSATION47 reports
DECREASED APPETITE47 reports
GASTROINTESTINAL DISORDER46 reports
MIGRAINE46 reports
TREMOR46 reports
DRUG EFFECT INCOMPLETE45 reports
JOINT SWELLING45 reports
OROPHARYNGEAL PAIN45 reports
STRESS45 reports
SWELLING45 reports
BRONCHITIS44 reports
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION44 reports
SEPSIS44 reports
NEUTROPHIL COUNT DECREASED43 reports
CONSTIPATION42 reports
DYSPNOEA EXERTIONAL41 reports
EAR INFECTION41 reports
HYPOAESTHESIA41 reports
NASAL CONGESTION40 reports
ABDOMINAL DISCOMFORT39 reports
MATERNAL EXPOSURE DURING PREGNANCY39 reports
MYALGIA39 reports
PLATELET COUNT DECREASED38 reports
PRODUCT QUALITY ISSUE38 reports
INFUSION SITE PAIN37 reports
LOSS OF CONSCIOUSNESS37 reports
PRODUCTIVE COUGH36 reports
SEIZURE36 reports
SOMNOLENCE36 reports
WHEEZING36 reports
EXPOSURE DURING PREGNANCY35 reports

Demographics Breakdown

Reports by Sex

Female2,559 (62.4%)
Male1,541 (37.6%)
Unknown2 (0.0%)

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 WATER?

This profile reflects 9,176 FDA FAERS reports that mention WATER. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for WATER?

Frequently reported terms in FAERS include HEREDITARY ANGIOEDEMA, FATIGUE, NAUSEA, HEADACHE, PRODUCT DOSE OMISSION ISSUE, PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

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.