Year: 2018. The FDA Adverse Event Reporting System (FAERS) registered 71 drug adverse reports.
|
| Month |
Report ID(s) |
Medicinal Product(s) |
Generic Name(s) |
Brand Name(s) |
Product NDC(s) |
Package NDC(s) |
| 12 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 11 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 10 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 09 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 08 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 07 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 06 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 05 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 04 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 03 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 02 |
|
|
|
|
|
|
| 01 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
Year: 2017. The FDA Adverse Event Reporting System (FAERS) registered 44 drug adverse reports.
|
| Month |
Report ID(s) |
Medicinal Product(s) |
Generic Name(s) |
Brand Name(s) |
Product NDC(s) |
Package NDC(s) |
| 12 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 11 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 10 |
|
|
- AMOXICILLIN AND CLAVULANATE POTASSIUM
- PIRFENIDONE
|
|
- 43598-004
- 43598-006
- 43598-012
- 43598-018
- 43598-021
- 50242-121
- 50242-122
- 50242-123
- 64116-121
- 72508-004
- 72508-006
- 72508-012
- 72508-018
- 72508-021
|
|
| 09 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 08 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 07 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 06 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 05 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|
| 01 |
|
|
|
|
- 50242-121
- 50242-122
- 50242-123
- 64116-121
|
|