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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127238331 | 12723833 | 1 | I | 201608 | 20160816 | 20160908 | 20160908 | PER | US-009507513-1608USA010550 | MERCK | 79.07 | YR | M | Y | 0.00000 | 20160908 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127238331 | 12723833 | 1 | PS | DECADRON | DEXAMETHASONE | 1 | 10 MG, QD | Y | 14694 | 10 | MG | INJECTION | QD | ||||||
| 127238331 | 12723833 | 2 | C | ADENOSINE. | ADENOSINE | 1 | Intravenous (not otherwise specified) | 12 MG, ONCE | 0 | 12 | MG | 1X |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127238331 | 12723833 | 1 | Pain |
| 127238331 | 12723833 | 2 | Supraventricular tachycardia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127238331 | 12723833 | Decreased appetite | |
| 127238331 | 12723833 | Insomnia | |
| 127238331 | 12723833 | Nausea |
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 |
|---|---|---|---|---|---|---|
| 127238331 | 12723833 | 1 | 20160811 | 20160814 | 0 | |
| 127238331 | 12723833 | 2 | 20160815 | 20160815 | 0 |