Minocycline
Common brands: Amzeeq, Zilxi, Prednisone, Prednisone Delayed Release, Prednisone Tablets, Usp, 10 Mg
Top reporter: Journey Medical Corporation
Corticosteroid [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Tumor Necrosis Factor Blocker [EPC]Folate Analog Metabolic Inhibitor [EPC]Antirheumatic Agent [EPC]
11,429
Total Reports
4,706
Serious Reports
1,549
Death Reports
30
Reported Reactions
Death Report Ratio: High (13.55%)
Patient Demographics
Reported Adverse Reactions (30)
Side effects reported in FDA adverse event reports for Minocycline.
| # | Reaction | Reports | % of Total |
|---|---|---|---|
| 1 | DRUG INEFFECTIVE | 1,925 | |
| 2 | OFF LABEL USE | 1,431 | |
| 3 | NAUSEA | 1,043 | |
| 4 | PAIN | 997 | |
| 5 | ARTHRALGIA | 968 | |
| 6 | FATIGUE | 924 | |
| 7 | DRUG INTOLERANCE | 881 | |
| 8 | RASH | 879 | |
| 9 | DRUG HYPERSENSITIVITY | 876 | |
| 10 | RHEUMATOID ARTHRITIS | 845 | |
| 11 | JOINT SWELLING | 844 | |
| 12 | HEADACHE | 781 | |
| 13 | CONDITION AGGRAVATED | 730 | |
| 14 | PNEUMONIA | 726 | |
| 15 | DIARRHOEA | 719 | |
| 16 | GENERAL PHYSICAL HEALTH DETERIORATION | 663 | |
| 17 | DIZZINESS | 662 | |
| 18 | HYPERTENSION | 645 | |
| 19 | C-REACTIVE PROTEIN INCREASED | 602 | |
| 20 | ABDOMINAL DISCOMFORT | 600 | |
| 21 | URTICARIA | 594 | |
| 22 | MALAISE | 588 | |
| 23 | TREATMENT FAILURE | 587 | |
| 24 | PAIN IN EXTREMITY | 586 | |
| 25 | PRODUCT USE IN UNAPPROVED INDICATION | 570 | |
| 26 | HEPATIC ENZYME INCREASED | 569 | |
| 27 | DEPRESSION | 568 | |
| 28 | OSTEOARTHRITIS | 567 | |
| 29 | VOMITING | 560 | |
| 30 | ALOPECIA | 555 |
Important Disclaimer
FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.