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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 77590972 | 7759097 | 2 | F | 20121219 | 20110113 | 20121231 | EXP | DK-RANBAXY-2010R1-40879 | RANBAXY | 28.00 | YR | M | Y | 0.00000 | 20121231 | OT | DK | DK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 77590972 | 7759097 | 1 | PS | PARACETAMOL | 1 | UNKNOWN | 2 G DAILY | D | 76200 | ||||||||||
| 77590972 | 7759097 | 2 | SS | Tramadol | 1 | UNKNOWN | 100 MG DAILY (20 DAYS A MONTH) | D | 0 | ||||||||||
| 77590972 | 7759097 | 3 | SS | Tolfenamic Acid | 1 | UNKNOWN | 300 MG DAILY (20 DAYS A MONTH) | D | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 77590972 | 7759097 | 1 | Headache |
| 77590972 | 7759097 | 2 | Headache |
| 77590972 | 7759097 | 3 | Headache |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 77590972 | 7759097 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 77590972 | 7759097 | Headache |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |