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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126575702 | 12657570 | 2 | F | 20160721 | 20160825 | 20160816 | 20160906 | EXP | US-MYLANLABS-2016M1033772 | MYLAN | 0.00 | Y | 0.00000 | 20160906 | CN | US | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126575702 | 12657570 | 1 | PS | EPINEPHRINE. | EPINEPHRINE | 1 | UNK | 19430 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126575702 | 12657570 | 1 | Hypersensitivity |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126575702 | 12657570 | Dizziness | |
| 126575702 | 12657570 | Dysgeusia | |
| 126575702 | 12657570 | Dyspnoea | |
| 126575702 | 12657570 | Epistaxis | |
| 126575702 | 12657570 | Headache | |
| 126575702 | 12657570 | Hypersensitivity | |
| 126575702 | 12657570 | Hypertension | |
| 126575702 | 12657570 | Palpitations | |
| 126575702 | 12657570 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 126575702 | 12657570 | 1 | 20160721 | 20160721 | 0 |