Year: 2019. The FDA Adverse Event Reporting System (FAERS) registered 7 drug adverse reports.
|
| Month |
Report ID(s) |
Medicinal Product(s) |
Generic Name(s) |
Brand Name(s) |
Product NDC(s) |
Package NDC(s) |
| 02 |
|
- AZITHROMYCIN MONOHYDRATE.
- ZITHROMAC SR 2G
|
|
- AZASITE
- AZITHROMYCIN
- AZITHROMYCIN MONOHYDRATE
|
- 0093-7148
- 0093-7149
- 17478-307
- 48792-7869
- 48792-7870
- 48792-7871
- 57297-162
- 63323-398
- 65162-708
- 65162-758
- 65162-759
- 65162-760
- 68083-199
- 68180-160
- 68180-161
- 68180-162
- 70860-100
|
|
| 01 |
|
- AZI-TEVA 500 MG FILMTABLETTEN
- AZITHROMYCIN MONOHYDRATE.
- AZITHROMYCINE MONOHYDRAT?E
- ZITHROMAC SR 2G
|
|
- AZASITE
- AZITHROMYCIN
- AZITHROMYCIN MONOHYDRATE
|
- 0093-7148
- 0093-7149
- 17478-307
- 48792-7869
- 48792-7870
- 48792-7871
- 57297-162
- 63323-398
- 65162-708
- 65162-758
- 65162-759
- 65162-760
- 68083-199
- 68180-160
- 68180-161
- 68180-162
- 70860-100
|
|