PHOSPHORIC ACID

N/A

Manufactured by BM Private Limited

3,032 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PHOSPHORIC ACID

PHOSPHORIC ACID is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by BM Private Limited. The most commonly reported adverse reactions for PHOSPHORIC ACID include CONSTIPATION, BALANCE DISORDER, ORTHOSTATIC HYPOTENSION, MOBILITY DECREASED, PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PHOSPHORIC ACID.

Top Adverse Reactions

CONSTIPATION135 reports
BALANCE DISORDER128 reports
ORTHOSTATIC HYPOTENSION113 reports
MOBILITY DECREASED110 reports
PAIN109 reports
BLOOD CALCIUM DECREASED103 reports
COGNITIVE DISORDER103 reports
CREATININE RENAL CLEARANCE DECREASED103 reports
DEPRESSED LEVEL OF CONSCIOUSNESS100 reports
FALL97 reports
HYPOTENSION92 reports
SEDATION92 reports
SEDATION COMPLICATION91 reports
DYSPNOEA87 reports
TOXICITY TO VARIOUS AGENTS77 reports
GAIT DISTURBANCE56 reports
PRODUCT USE IN UNAPPROVED INDICATION55 reports
OFF LABEL USE47 reports
DRUG INTERACTION41 reports
ANAEMIA40 reports
NAUSEA40 reports
DEATH37 reports
HEADACHE37 reports
DECREASED APPETITE36 reports
DIARRHOEA36 reports
VOMITING36 reports
ASTHENIA34 reports
HYPOKALAEMIA34 reports
HYPOMAGNESAEMIA34 reports
NEUTROPENIC SEPSIS34 reports
DEHYDRATION33 reports
DYSPHAGIA33 reports
MOUTH ULCERATION33 reports
MUCOSAL INFLAMMATION33 reports
PRODUCTIVE COUGH33 reports
RENAL FUNCTION TEST ABNORMAL33 reports
SKIN CANDIDA33 reports
DEPRESSION32 reports
OVERDOSE31 reports
NERVOUS SYSTEM DISORDER30 reports
NEUTROPHIL COUNT DECREASED30 reports
DRUG ABUSE29 reports
MULTIPLE DRUG THERAPY29 reports
DRUG INEFFECTIVE27 reports
RHEUMATOID ARTHRITIS26 reports
BLADDER DISORDER23 reports
CREATININE RENAL CLEARANCE INCREASED23 reports
CONDITION AGGRAVATED22 reports
SCIATICA20 reports
CANDIDA INFECTION19 reports
CONTRAINDICATED PRODUCT ADMINISTERED19 reports
HAND DEFORMITY19 reports
INJECTION SITE REACTION19 reports
TREATMENT FAILURE15 reports
DEMENTIA13 reports
PRODUCT USE ISSUE12 reports
DEFORMITY11 reports
FATIGUE11 reports
DRUG INTOLERANCE8 reports
SOMNOLENCE8 reports
VISUAL IMPAIRMENT8 reports
HYPOAESTHESIA7 reports
ABDOMINAL PAIN6 reports
ALOPECIA6 reports
CONTUSION6 reports
CYTOKINE RELEASE SYNDROME6 reports
DIZZINESS6 reports
INSOMNIA6 reports
METASTASES TO BONE6 reports
PAIN IN EXTREMITY6 reports
THROMBOCYTOPENIA6 reports
AGEUSIA5 reports
COMPLETED SUICIDE5 reports
ERYTHEMA5 reports
MALAISE5 reports
MUSCULAR WEAKNESS5 reports
NEUTROPENIA5 reports
ORAL CANDIDIASIS5 reports
PERIPHERAL COLDNESS5 reports
ARTERIOSCLEROSIS4 reports
ARTHROPATHY4 reports
BRAIN OEDEMA4 reports
CARDIAC FAILURE4 reports
CARDIOPULMONARY FAILURE4 reports
CEREBRAL CONGESTION4 reports
CONJUNCTIVAL HAEMORRHAGE4 reports
HAEMOTHORAX4 reports
HYPERAEMIA4 reports
ILL DEFINED DISORDER4 reports
LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES4 reports
MYOCARDIAL INFARCTION4 reports
OEDEMA4 reports
PULMONARY CONGESTION4 reports
PULMONARY OEDEMA4 reports
SWELLING4 reports
ACUTE KIDNEY INJURY3 reports
CHILLS3 reports
CONFUSIONAL STATE3 reports
INTENTIONAL PRODUCT USE ISSUE3 reports
MYOCARDIAL ISCHAEMIA3 reports

Report Outcomes

Out of 235 classified reports for PHOSPHORIC ACID:

Serious 98.7%Non-Serious 1.3%

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

Female169 (88.9%)
Male21 (11.1%)

Reports by Age

Age 7785 reports
Age 7140 reports
Age 7416 reports
Age 415 reports
Age 575 reports
Age 554 reports
Age 463 reports
Age 262 reports
Age 522 reports
Age 682 reports
Age 732 reports
Age 41 reports
Age 71 reports
Age 91 reports
Age 111 reports
Age 121 reports
Age 341 reports
Age 401 reports
Age 421 reports
Age 621 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 PHOSPHORIC ACID?

This profile reflects 3,032 FDA FAERS reports that mention PHOSPHORIC ACID. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PHOSPHORIC ACID?

Frequently reported terms in FAERS include CONSTIPATION, BALANCE DISORDER, ORTHOSTATIC HYPOTENSION, MOBILITY DECREASED, PAIN, BLOOD CALCIUM DECREASED. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PHOSPHORIC ACID?

Labeling and FAERS entries often list BM Private Limited in connection with PHOSPHORIC ACID. 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.