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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 92006531 | 9200653 | 1 | I | 20121221 | 20130319 | 20130331 | 20130331 | EXP | GB-TEVA-393160ISR | TEVA | 39.00 | YR | M | Y | 74.00000 | KG | 20130331 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 92006531 | 9200653 | 1 | PS | CIPROFLOXACIN | 1 | U | 74124 | 250 | MG | ||||||||||
| 92006531 | 9200653 | 2 | C | AMOXICILLIN | 1 | D | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 92006531 | 9200653 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 92006531 | 9200653 | Abdominal discomfort | |
| 92006531 | 9200653 | Food intolerance | |
| 92006531 | 9200653 | Tendon disorder | |
| 92006531 | 9200653 | Visual impairment |
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 |
|---|---|---|---|---|---|---|
| 92006531 | 9200653 | 1 | 20121217 | 20121226 | 0 | |
| 92006531 | 9200653 | 2 | 20121213 | 20121218 | 0 |