.ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D

N/A

Manufactured by Method Pharmaceuticals, LLC

470 FDA adverse event reports analyzed

Last updated: 2026-04-15

About .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D

.ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Method Pharmaceuticals, LLC. The most commonly reported adverse reactions for .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D include RASH, FATIGUE, FLUSHING, ARTHRALGIA, COUGH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D.

Top Adverse Reactions

RASH16 reports
FATIGUE13 reports
FLUSHING12 reports
ARTHRALGIA11 reports
COUGH11 reports
NAUSEA11 reports
DIZZINESS10 reports
OFF LABEL USE10 reports
ABDOMINAL PAIN9 reports
DIARRHOEA9 reports
DYSPNOEA9 reports
HYPERSENSITIVITY9 reports
PRURITUS9 reports
DEATH8 reports
HEADACHE8 reports
RASH ERYTHEMATOUS8 reports
URTICARIA8 reports
ADVERSE DRUG REACTION7 reports
VOMITING7 reports
CONDITION AGGRAVATED6 reports
DECREASED APPETITE6 reports
ERYTHEMA6 reports
INSOMNIA6 reports
MALAISE6 reports
PNEUMONIA6 reports
PRODUCT DOSE OMISSION ISSUE6 reports
PRODUCT SUBSTITUTION ISSUE6 reports
ABDOMINAL DISCOMFORT5 reports
ABDOMINAL PAIN UPPER5 reports
COVID 195 reports
DRUG INEFFECTIVE5 reports
FALL5 reports
HOSPITALISATION5 reports
INFLUENZA5 reports
MEMORY IMPAIRMENT5 reports
PAIN5 reports
PRODUCT USE ISSUE5 reports
PYREXIA5 reports
SEIZURE5 reports
BLOOD IRON DECREASED4 reports
CONTUSION4 reports
CRYING4 reports
CYSTIC FIBROSIS4 reports
DERMATITIS ATOPIC4 reports
DISCOMFORT4 reports
DRY SKIN4 reports
FEELING HOT4 reports
INCORRECT DOSE ADMINISTERED4 reports
INJECTION SITE PAIN4 reports
MUSCLE SPASMS4 reports
PERIPHERAL SWELLING4 reports
SINUSITIS4 reports
SOMNOLENCE4 reports
THERAPY NON RESPONDER4 reports
BALANCE DISORDER3 reports
CONFUSIONAL STATE3 reports
CONSTIPATION3 reports
DYSPEPSIA3 reports
EYE IRRITATION3 reports
FEELING ABNORMAL3 reports
HAEMOGLOBIN DECREASED3 reports
HERPES ZOSTER3 reports
HYPOAESTHESIA3 reports
HYPOTENSION3 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION3 reports
LABORATORY TEST ABNORMAL3 reports
MUSCULOSKELETAL STIFFNESS3 reports
PAIN IN EXTREMITY3 reports
PLATELET COUNT DECREASED3 reports
PRODUCT COMPLAINT3 reports
PRODUCT DOSE OMISSION3 reports
PRODUCT FORMULATION ISSUE3 reports
RASH MACULAR3 reports
RHINORRHOEA3 reports
THROAT IRRITATION3 reports
WEIGHT INCREASED3 reports
WHITE BLOOD CELL COUNT DECREASED3 reports
WOUND INFECTION3 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS3 reports
ABDOMINAL DISTENSION2 reports
ACCIDENTAL EXPOSURE TO PRODUCT2 reports
ACNE2 reports
ADVERSE REACTION2 reports
ASTHENIA2 reports
BACK PAIN2 reports
BONE PAIN2 reports
BURNING SENSATION2 reports
CATARACT2 reports
COMPLICATION OF DEVICE INSERTION2 reports
DEHYDRATION2 reports
DRUG INTOLERANCE2 reports
DYSGEUSIA2 reports
DYSPHAGIA2 reports
EXTERNAL EAR INFLAMMATION2 reports
GASTROOESOPHAGEAL REFLUX DISEASE2 reports
HAEMORRHAGE2 reports
HEART RATE INCREASED2 reports
HOT FLUSH2 reports
HYPOACUSIS2 reports
HYPOKINESIA2 reports

Report Outcomes

Out of 200 classified reports for .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D:

Serious 48.0%Non-Serious 52.0%

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

Female103 (58.5%)
Male73 (41.5%)

Reports by Age

Age 28 reports
Age 37 reports
Age 57 reports
Age 96 reports
Age 845 reports
Age 44 reports
Age 74 reports
Age 84 reports
Age 104 reports
Age 744 reports
Age 754 reports
Age 143 reports
Age 393 reports
Age 603 reports
Age 733 reports
Age 12 reports
Age 62 reports
Age 122 reports
Age 302 reports
Age 332 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 .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D?

This profile reflects 470 FDA FAERS reports that mention .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D?

Frequently reported terms in FAERS include RASH, FATIGUE, FLUSHING, ARTHRALGIA, COUGH, NAUSEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D?

Labeling and FAERS entries often list Method Pharmaceuticals, LLC in connection with .ALPHA. TOCOPHEROL ACETATE, DL , ASCORBIC ACID, CYANOCOBALAMIN, FOLIC ACID, NIACIN, PYRIDOXINE, RIBOFLAVIN, SODIUM FLUORIDE, THIAMINE MONONITRATE, VITAMIN A AND VITAMIN D. 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.