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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127279291 | 12727929 | 1 | I | 20160827 | 20160909 | 20160909 | EXP | TR-VALIDUS PHARMACEUTICALS LLC-TR-2016VAL002594 | VALIDUS | ARICI MA, GIRGIN MC, YANTURALI S, ORAY NC, DOYLAN O, DEMIRAL Y ET AL. EMERGENCY DEPARTMENT VISITS CAUSED BY ADVERSE DRUG REACTIONS: RESULTS OF A TURKISH UNIVERSITY HOSPITAL. TURKISH JOURNAL OF MEDICAL SCIENCES. 2016;46:945-52 | 0.00 | Y | 0.00000 | 20160909 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127279291 | 12727929 | 1 | PS | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | UNK | U | 17963 | ||||||||||
| 127279291 | 12727929 | 2 | SS | ETODOLAC. | ETODOLAC | 1 | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127279291 | 12727929 | 1 | Product used for unknown indication |
| 127279291 | 12727929 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127279291 | 12727929 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127279291 | 12727929 | Drug interaction | |
| 127279291 | 12727929 | Hypertension |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |