POTASSIUM NITRATE

N/A

437 FDA adverse event reports analyzed

Last updated: 2026-04-15

About POTASSIUM NITRATE

POTASSIUM NITRATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for POTASSIUM NITRATE include DRUG INEFFECTIVE, ORAL DISCOMFORT, HYPERAESTHESIA TEETH, TOOTHACHE, CONDITION AGGRAVATED. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for POTASSIUM NITRATE.

Top Adverse Reactions

DRUG INEFFECTIVE41 reports
ORAL DISCOMFORT31 reports
HYPERAESTHESIA TEETH16 reports
TOOTHACHE15 reports
CONDITION AGGRAVATED14 reports
ORAL PAIN12 reports
ORAL MUCOSAL EXFOLIATION11 reports
STOMATITIS10 reports
HYPERSENSITIVITY9 reports
PRODUCT COMPLAINT8 reports
PRODUCT USE IN UNAPPROVED INDICATION8 reports
TONGUE DISCOMFORT8 reports
GINGIVAL PAIN7 reports
GLOSSODYNIA7 reports
LIP SWELLING7 reports
DERMATITIS CONTACT6 reports
DYSGEUSIA5 reports
GINGIVAL DISCOMFORT5 reports
THROAT IRRITATION5 reports
ACCIDENTAL EXPOSURE TO PRODUCT4 reports
CHOKING4 reports
COUGH4 reports
DIARRHOEA4 reports
DRUG EFFECT LESS THAN EXPECTED4 reports
DRUG EFFECTIVE FOR UNAPPROVED INDICATION4 reports
DRY MOUTH4 reports
DYSPEPSIA4 reports
GINGIVAL SWELLING4 reports
HEADACHE4 reports
NONINFECTIVE GINGIVITIS4 reports
TOOTH DISORDER4 reports
ADVERSE DRUG REACTION3 reports
AGEUSIA3 reports
ALOPECIA3 reports
ANAPHYLACTIC REACTION3 reports
BLOOD PRESSURE INCREASED3 reports
COATING IN MOUTH3 reports
CONSTIPATION3 reports
DENTAL DISCOMFORT3 reports
DRUG HYPERSENSITIVITY3 reports
EXPIRED PRODUCT ADMINISTERED3 reports
FATIGUE3 reports
GINGIVAL BLEEDING3 reports
GINGIVAL DISORDER3 reports
HAEMORRHAGE3 reports
HYPOAESTHESIA ORAL3 reports
ILL DEFINED DISORDER3 reports
ILLNESS3 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION3 reports
LIP DRY3 reports
NAUSEA3 reports
OROPHARYNGEAL PAIN3 reports
PAIN3 reports
SWELLING FACE3 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE3 reports
THERAPEUTIC RESPONSE UNEXPECTED3 reports
TOOTH INJURY3 reports
ABDOMINAL DISTENSION2 reports
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED2 reports
ARTHRALGIA2 reports
BURN ORAL CAVITY2 reports
BURNING SENSATION2 reports
DEATH2 reports
DENTAL CARIES2 reports
DISCOMFORT2 reports
DRUG DEPENDENCE2 reports
DRUG INTERACTION2 reports
DRY SKIN2 reports
FACIAL PARALYSIS2 reports
FOAMING AT MOUTH2 reports
INTERVERTEBRAL DISC PROTRUSION2 reports
LIP BLISTER2 reports
LIP PAIN2 reports
MACULAR DEGENERATION2 reports
MALAISE2 reports
MOUTH SWELLING2 reports
MOUTH ULCERATION2 reports
NASOPHARYNGITIS2 reports
ORAL CONTUSION2 reports
ORAL DISORDER2 reports
ORAL MUCOSAL ERYTHEMA2 reports
OROPHARYNGEAL DISCOMFORT2 reports
PAIN IN EXTREMITY2 reports
PAIN IN JAW2 reports
PARAESTHESIA2 reports
PHARYNGEAL OEDEMA2 reports
PRODUCT PACKAGE ASSOCIATED INJURY2 reports
PRODUCT QUALITY ISSUE2 reports
PYREXIA2 reports
RASH2 reports
RHINORRHOEA2 reports
SEIZURE2 reports
SENSATION OF FOREIGN BODY2 reports
SENSITIVITY OF TEETH2 reports
SKIN EXFOLIATION2 reports
SWOLLEN TONGUE2 reports
THROAT TIGHTNESS2 reports
TONGUE BLISTERING2 reports
TONGUE EXFOLIATION2 reports
TOOTH DISCOLOURATION2 reports

Demographics Breakdown

Reports by Sex

Female78 (66.7%)
Male39 (33.3%)

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 POTASSIUM NITRATE?

This profile reflects 437 FDA FAERS reports that mention POTASSIUM NITRATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for POTASSIUM NITRATE?

Frequently reported terms in FAERS include DRUG INEFFECTIVE, ORAL DISCOMFORT, HYPERAESTHESIA TEETH, TOOTHACHE, CONDITION AGGRAVATED, ORAL 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.