VITAMIN D3 Adverse Event: Forced expiratory volume decreased
VITAMIN D3 Adverse Event: Forced expiratory volume decreased is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: VITAMIN D3; Product category: Drug; Primary reaction: Forced expiratory volume decreased.
| Primary drug | VITAMIN D3 |
|---|---|
| Product category | Drug |
| Primary reaction | Forced expiratory volume decreased |
| All reactions | Forced expiratory volume decreased |
| Seriousness | Serious |
| Patient outcome | Recovered/Resolved |
| Patient sex | Female |
| All drugs reported | VITAMIN D3; NEXIUM; TOBI; ZOLOFT |
| Reporter country | US |
| Reporter type | 1 |
| Report date | 20140313 |
| Report ID | 10006429 |
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