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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127388511 | 12738851 | 1 | I | 20160829 | 20160912 | 20160912 | EXP | TR-IPCA LABORATORIES LIMITED-IPC201609-000737 | IPCA | GIRGIN M,YANTURALI S,ARICI M,COLAK ORAY N,DOYLAN O,DEMIRAL Y. EMERGENCY DEPARTMENT VISITS CAUSED BY ADVERSE DRUG REACTIONS: RESULTS OF A TURKISH UNIVERSITY HOSPITAL. TURK J MED SCI 2016 JUN 23;46(4):945-52. | 0.00 | E | Y | 0.00000 | 20160912 | OT | TR | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127388511 | 12738851 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | U | 78459 | |||||||||||
| 127388511 | 12738851 | 2 | SS | ETODOLAC. | ETODOLAC | 1 | U | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127388511 | 12738851 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127388511 | 12738851 | Drug interaction | |
| 127388511 | 12738851 | Hypertension |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |