THYROID, PORCINE

N/A

Manufactured by Allergan, Inc.

22,624 FDA adverse event reports analyzed

Last updated: 2026-04-14

About THYROID, PORCINE

THYROID, PORCINE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Allergan, Inc.. The most commonly reported adverse reactions for THYROID, PORCINE include FATIGUE, DRUG INEFFECTIVE, HEADACHE, NAUSEA, PAIN. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for THYROID, PORCINE.

Top Adverse Reactions

FATIGUE1,025 reports
DRUG INEFFECTIVE878 reports
HEADACHE783 reports
NAUSEA770 reports
PAIN570 reports
DIZZINESS536 reports
DIARRHOEA503 reports
OFF LABEL USE469 reports
FEELING ABNORMAL461 reports
ARTHRALGIA432 reports
MALAISE428 reports
ANXIETY421 reports
DYSPNOEA420 reports
INSOMNIA395 reports
ASTHENIA360 reports
ALOPECIA356 reports
WEIGHT INCREASED341 reports
RASH337 reports
PRURITUS323 reports
PALPITATIONS312 reports
FALL302 reports
DEPRESSION300 reports
WEIGHT DECREASED293 reports
VOMITING292 reports
PAIN IN EXTREMITY263 reports
CONDITION AGGRAVATED246 reports
BLOOD PRESSURE INCREASED244 reports
COUGH240 reports
CONSTIPATION230 reports
MUSCLE SPASMS227 reports
BACK PAIN226 reports
HYPERTENSION220 reports
TREMOR204 reports
PRODUCT DOSE OMISSION ISSUE196 reports
SINUSITIS194 reports
SOMNOLENCE194 reports
ABDOMINAL PAIN UPPER187 reports
PERIPHERAL SWELLING185 reports
MYALGIA183 reports
GAIT DISTURBANCE182 reports
HEART RATE INCREASED182 reports
COVID 19179 reports
URINARY TRACT INFECTION176 reports
ABDOMINAL DISCOMFORT173 reports
HYPERHIDROSIS172 reports
INJECTION SITE PAIN171 reports
NASOPHARYNGITIS170 reports
PARAESTHESIA170 reports
PYREXIA170 reports
VISION BLURRED170 reports
CHEST PAIN169 reports
URTICARIA168 reports
HYPERSENSITIVITY167 reports
MIGRAINE166 reports
PRODUCT QUALITY ISSUE165 reports
HYPOAESTHESIA162 reports
DRUG HYPERSENSITIVITY159 reports
MEMORY IMPAIRMENT157 reports
PNEUMONIA157 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS156 reports
PRODUCT SUBSTITUTION ISSUE149 reports
ILLNESS147 reports
ERYTHEMA144 reports
ABDOMINAL PAIN142 reports
DECREASED APPETITE142 reports
INCORRECT DOSE ADMINISTERED138 reports
DRUG DOSE OMISSION137 reports
UNEVALUABLE EVENT136 reports
ABDOMINAL DISTENSION133 reports
PRODUCT USE ISSUE126 reports
HYPOTHYROIDISM125 reports
PRODUCT USE IN UNAPPROVED INDICATION125 reports
JOINT SWELLING124 reports
MUSCULAR WEAKNESS124 reports
HOT FLUSH118 reports
DRY SKIN116 reports
BRONCHITIS115 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION112 reports
OROPHARYNGEAL PAIN110 reports
DEHYDRATION108 reports
DEATH106 reports
DYSPEPSIA104 reports
EYE PAIN103 reports
VISUAL IMPAIRMENT103 reports
CONFUSIONAL STATE102 reports
ARTHRITIS101 reports
CHILLS101 reports
GASTROOESOPHAGEAL REFLUX DISEASE101 reports
NECK PAIN101 reports
NEUROPATHY PERIPHERAL100 reports
ATRIAL FIBRILLATION98 reports
CHEST DISCOMFORT98 reports
DRY MOUTH97 reports
CONTUSION95 reports
ADVERSE DRUG REACTION94 reports
BLOOD THYROID STIMULATING HORMONE INCREASED94 reports
BALANCE DISORDER93 reports
STRESS93 reports
DRUG INTOLERANCE91 reports
THERAPEUTIC RESPONSE UNEXPECTED91 reports

Report Outcomes

Out of 10,152 classified reports for THYROID, PORCINE:

Serious 42.9%Non-Serious 57.1%

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

Female8,498 (90.3%)
Male900 (9.6%)
Unknown14 (0.1%)

Reports by Age

Age 61199 reports
Age 62187 reports
Age 59169 reports
Age 58163 reports
Age 56162 reports
Age 63162 reports
Age 65161 reports
Age 55159 reports
Age 67159 reports
Age 60158 reports
Age 64157 reports
Age 57155 reports
Age 71154 reports
Age 53150 reports
Age 66147 reports
Age 68145 reports
Age 69135 reports
Age 54127 reports
Age 70120 reports
Age 51118 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 THYROID, PORCINE?

This profile reflects 22,624 FDA FAERS reports that mention THYROID, PORCINE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for THYROID, PORCINE?

Frequently reported terms in FAERS include FATIGUE, DRUG INEFFECTIVE, HEADACHE, NAUSEA, PAIN, DIZZINESS. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures THYROID, PORCINE?

Labeling and FAERS entries often list Allergan, Inc. in connection with THYROID, PORCINE. 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.