Year: 2018. The FDA Adverse Event Reporting System (FAERS) registered 9 drug adverse reports.
|
| Month |
Report ID(s) |
Medicinal Product(s) |
Generic Name(s) |
Brand Name(s) |
Product NDC(s) |
Package NDC(s) |
| 12 |
|
|
|
|
- 70709-000
- 70709-002
- 70709-005
|
|
| 11 |
|
|
|
|
- 66658-102
- 66658-105
- 66658-110
- 66658-120
- 66658-204
|
|
| 06 |
|
|
|
|
- 66658-102
- 66658-105
- 66658-110
- 66658-120
- 66658-204
|
|
| 04 |
|
|
|
|
- 66658-102
- 66658-105
- 66658-110
- 66658-120
- 66658-204
- 70709-000
- 70709-002
- 70709-005
|
|