Year: 2019. The FDA Adverse Event Reporting System (FAERS) registered 12 drug adverse reports.
|
| Month |
Report ID(s) |
Medicinal Product(s) |
Generic Name(s) |
Brand Name(s) |
Product NDC(s) |
Package NDC(s) |
| 03 |
|
- EQ MICON 7 DISPOSAL
- EQ MICONAZOLE 3
- MICONAZOLE 2%
- MICONAZOLE.
- ORAVIG
|
- ANTIFUNGAL
- MICONAZOLE
- MICONAZOLE NITRATE
|
- DYNAREX ANTIFUNGAL POWDER
- MAKESENSE
- MICONAZOLE
- MICONAZOLE 1
- MICONAZOLE 1 FEMININE CARE
- MICONAZOLE 1 YEAST INFECTION RELIEF
- MICONAZOLE 3
- MICONAZOLE 7
- ORAVIG
- RASH RELIEF ANTIFUNGAL
|
- 0363-0081
- 0363-0199
- 0363-0637
- 0363-0730
- 0363-0737
- 0363-0916
- 0363-2070
- 0472-0730
- 0472-1736
- 0904-7734
- 11822-0199
- 11822-0730
- 11822-0737
- 11822-0800
- 11822-0916
- 11822-0982
- 15071-804
- 30142-081
- 30142-199
- 30142-737
- 30142-825
- 30142-982
- 37012-035
- 37012-070
- 37808-199
- 37808-242
- 37808-737
- 37808-825
- 41250-081
- 41250-199
- 41250-737
- 41250-825
- 41250-982
- 49035-730
- 49348-833
- 49781-064
- 50382-050
- 55319-730
- 59779-199
- 59779-737
- 59779-839
- 61715-050
- 63868-198
- 67777-316
- 68016-073
- 68016-291
- 69020-208
- 69842-950
- 69842-988
- 89141-250
|
|
| 02 |
|
|
- ANTIFUNGAL
- MICONAZOLE
- MICONAZOLE NITRATE
|
- DYNAREX ANTIFUNGAL POWDER
- MAKESENSE
- MICONAZOLE
- ORAVIG
- RASH RELIEF ANTIFUNGAL
|
- 15071-804
- 50382-050
- 61715-050
- 67777-316
- 68016-291
- 69020-208
- 89141-250
|
|
| 01 |
|
- EQ MICONAZOLE 3
- MICONAZOLE.
|
- ANTIFUNGAL
- MICONAZOLE
- MICONAZOLE NITRATE
|
- DYNAREX ANTIFUNGAL POWDER
- MAKESENSE
- MICONAZOLE
- ORAVIG
- RASH RELIEF ANTIFUNGAL
|
- 15071-804
- 50382-050
- 61715-050
- 67777-316
- 68016-291
- 69020-208
- 89141-250
|
|