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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114344952 | 11434495 | 2 | F | 20160721 | 20150831 | 20160803 | PER | US-BAYER-2015-403692 | BAYER | 0.00 | A | F | Y | 61.22000 | KG | 20160803 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 114344952 | 11434495 | 1 | PS | AVELOX | MOXIFLOXACIN HYDROCHLORIDE | 1 | 400 MG, UNK | 21085 | 400 | MG | FILM-COATED TABLET |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 114344952 | 11434495 | Anxiety | |
| 114344952 | 11434495 | Burning sensation | |
| 114344952 | 11434495 | Emotional distress | |
| 114344952 | 11434495 | Hypoaesthesia | |
| 114344952 | 11434495 | Injury | |
| 114344952 | 11434495 | Muscular weakness | |
| 114344952 | 11434495 | Neuropathy peripheral | |
| 114344952 | 11434495 | Pain | |
| 114344952 | 11434495 | Pain in extremity | |
| 114344952 | 11434495 | Paraesthesia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 114344952 | 11434495 | 1 | 201305 | 0 |