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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127619581 | 12761958 | 1 | I | 20160906 | 20160920 | 20160920 | EXP | PHHY2016US128780 | SANDOZ | 0.00 | F | Y | 0.00000 | 20160920 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127619581 | 12761958 | 1 | PS | METOPROLOL. | METOPROLOL | 1 | Unknown | UNK UNK, PRN | 73288 | ||||||||||
| 127619581 | 12761958 | 2 | C | ELIQUIS | APIXABAN | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127619581 | 12761958 | 1 | Blood pressure increased |
| 127619581 | 12761958 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127619581 | 12761958 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127619581 | 12761958 | Abdominal discomfort | |
| 127619581 | 12761958 | Cerebrovascular accident | |
| 127619581 | 12761958 | Depression | |
| 127619581 | 12761958 | Fear | |
| 127619581 | 12761958 | Feeling abnormal | |
| 127619581 | 12761958 | Hallucination | |
| 127619581 | 12761958 | Hypoaesthesia | |
| 127619581 | 12761958 | Malaise | |
| 127619581 | 12761958 | Nightmare |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |