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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127234252 | 12723425 | 2 | F | 2015 | 20160907 | 20160908 | 20160916 | EXP | US-009507513-1609USA000043 | MERCK | 0.00 | F | Y | 54.40000 | KG | 20160916 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127234252 | 12723425 | 1 | PS | SINEMET | CARBIDOPALEVODOPA | 1 | Oral | U | 17555 | TABLET | |||||||||
127234252 | 12723425 | 2 | SS | REQUIP | ROPINIROLE HYDROCHLORIDE | 1 | UNK | Y | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127234252 | 12723425 | 1 | Parkinson's disease |
127234252 | 12723425 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127234252 | 12723425 | HO |
127234252 | 12723425 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127234252 | 12723425 | Blood pressure decreased | |
127234252 | 12723425 | Condition aggravated | |
127234252 | 12723425 | Fatigue | |
127234252 | 12723425 | Loss of consciousness | |
127234252 | 12723425 | Miosis |
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 |
---|---|---|---|---|---|---|
127234252 | 12723425 | 2 | 2015 | 0 |