FLUORIDE

N/A

Manufactured by CVS Pharmacy

524 FDA adverse event reports analyzed

Last updated: 2026-04-15

About FLUORIDE

FLUORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by CVS Pharmacy. The most commonly reported adverse reactions for FLUORIDE include TOXICITY TO VARIOUS AGENTS, HEADACHE, COMPLETED SUICIDE, NAUSEA, ASTHENIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for FLUORIDE.

Top Adverse Reactions

TOXICITY TO VARIOUS AGENTS16 reports
HEADACHE15 reports
COMPLETED SUICIDE14 reports
NAUSEA13 reports
ASTHENIA12 reports
FATIGUE11 reports
INSOMNIA11 reports
DRUG INEFFECTIVE10 reports
DYSPNOEA10 reports
DIARRHOEA9 reports
MALAISE9 reports
VOMITING9 reports
CONSTIPATION8 reports
HYPERSENSITIVITY8 reports
PYREXIA8 reports
ABDOMINAL PAIN UPPER7 reports
ARTHRALGIA7 reports
DIZZINESS7 reports
MEMORY IMPAIRMENT7 reports
PRURITUS7 reports
RASH7 reports
AGGRESSION6 reports
ANXIETY6 reports
BACK PAIN6 reports
COUGH6 reports
INCORRECT DOSE ADMINISTERED6 reports
PAIN IN EXTREMITY6 reports
PARAESTHESIA6 reports
PLATELET COUNT DECREASED6 reports
PRODUCT QUALITY ISSUE6 reports
ABDOMINAL PAIN5 reports
ABNORMAL BEHAVIOUR5 reports
ANAEMIA5 reports
ANAPHYLACTIC REACTION5 reports
BLOOD ALKALINE PHOSPHATASE INCREASED5 reports
CONDITION AGGRAVATED5 reports
COVID 195 reports
GAIT DISTURBANCE5 reports
NIGHTMARE5 reports
OFF LABEL USE5 reports
OVERDOSE5 reports
PAIN5 reports
PNEUMONIA5 reports
SLEEP DISORDER5 reports
SOMNOLENCE5 reports
URINARY TRACT INFECTION5 reports
WEIGHT DECREASED5 reports
WEIGHT INCREASED5 reports
WHITE BLOOD CELL COUNT DECREASED5 reports
ABDOMINAL DISCOMFORT4 reports
ASPARTATE AMINOTRANSFERASE INCREASED4 reports
DEATH4 reports
DECREASED APPETITE4 reports
DISEASE RECURRENCE4 reports
FALL4 reports
FEELING HOT4 reports
HYPOAESTHESIA4 reports
HYPOTENSION4 reports
HYPOXIA4 reports
INFLUENZA4 reports
MEDICATION ERROR4 reports
NECK PAIN4 reports
RENAL FAILURE4 reports
SEPSIS4 reports
SINUSITIS4 reports
TREMOR4 reports
UNRESPONSIVE TO STIMULI4 reports
ABNORMAL DREAMS3 reports
ACNE3 reports
ALANINE AMINOTRANSFERASE INCREASED3 reports
BLOOD GLUCOSE INCREASED3 reports
CONTUSION3 reports
CYSTITIS3 reports
DEPRESSION3 reports
DRUG HYPERSENSITIVITY3 reports
DRY MOUTH3 reports
DYSKINESIA3 reports
FEBRILE NEUTROPENIA3 reports
FLUSHING3 reports
GENERAL PHYSICAL HEALTH DETERIORATION3 reports
HAEMORRHAGE3 reports
HYPERGLYCAEMIA3 reports
HYPOCALCAEMIA3 reports
HYPOGLYCAEMIA3 reports
IRRITABILITY3 reports
LYMPHOCYTE COUNT DECREASED3 reports
MIGRAINE3 reports
MUSCLE SPASMS3 reports
MUSCULAR WEAKNESS3 reports
NEUTROPHIL COUNT DECREASED3 reports
PERIPHERAL SWELLING3 reports
PLASMA CELL MYELOMA RECURRENT3 reports
PRODUCT USE IN UNAPPROVED INDICATION3 reports
PSYCHOMOTOR HYPERACTIVITY3 reports
RESTLESSNESS3 reports
RHINOVIRUS INFECTION3 reports
STOMACH DISCOMFORT3 reports
STOMATITIS3 reports
URTICARIA3 reports
ABDOMINAL PAIN LOWER2 reports

Report Outcomes

Out of 225 classified reports for FLUORIDE:

Serious 57.8%Non-Serious 42.2%

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

Female134 (61.2%)
Male84 (38.4%)
Unknown1 (0.5%)

Reports by Age

Age 4416 reports
Age 56 reports
Age 66 reports
Age 86 reports
Age 96 reports
Age 125 reports
Age 605 reports
Age 74 reports
Age 154 reports
Age 644 reports
Age 654 reports
Age 684 reports
Age 704 reports
Age 804 reports
Age 23 reports
Age 43 reports
Age 133 reports
Age 163 reports
Age 473 reports
Age 593 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 FLUORIDE?

This profile reflects 524 FDA FAERS reports that mention FLUORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for FLUORIDE?

Frequently reported terms in FAERS include TOXICITY TO VARIOUS AGENTS, HEADACHE, COMPLETED SUICIDE, NAUSEA, ASTHENIA, FATIGUE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures FLUORIDE?

Labeling and FAERS entries often list CVS Pharmacy in connection with FLUORIDE. 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.