Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120420923 | 12042092 | 3 | F | 20160803 | 20160208 | 20160815 | PER | US-BAYER-2016-022833 | BAYER | 54.00 | YR | A | M | Y | 99.77000 | KG | 20160815 | LW | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 120420923 | 12042092 | 1 | PS | CIPRO | CIPROFLOXACIN HYDROCHLORIDE | 1 | UNK | 19537 | TABLET | ||||||||||
| 120420923 | 12042092 | 2 | SS | AVELOX | MOXIFLOXACIN HYDROCHLORIDE | 1 | UNK | 0 | FILM-COATED TABLET | ||||||||||
| 120420923 | 12042092 | 3 | SS | LEVAQUIN | LEVOFLOXACIN | 1 | UNK | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 120420923 | 12042092 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 120420923 | 12042092 | Cardiovascular disorder | |
| 120420923 | 12042092 | Depression | |
| 120420923 | 12042092 | Mental disorder | |
| 120420923 | 12042092 | Musculoskeletal injury | |
| 120420923 | 12042092 | Nervous system disorder | |
| 120420923 | 12042092 | Neuropathy peripheral | |
| 120420923 | 12042092 | Pain | |
| 120420923 | 12042092 | Peripheral nerve injury | |
| 120420923 | 12042092 | Skin injury |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |