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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125593932 | 12559393 | 2 | F | 20160625 | 20160810 | 20160715 | 20160817 | EXP | FR-009507513-1607FRA005587 | MERCK | 77.62 | YR | M | Y | 0.00000 | 20160817 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125593932 | 12559393 | 1 | PS | SINEMET | CARBIDOPALEVODOPA | 1 | Oral | 0.5 DF, TID | Y | N | 17555 | .5 | DF | TABLET | TID | ||||
125593932 | 12559393 | 2 | SS | SINEMET | CARBIDOPALEVODOPA | 1 | Oral | HALF A TABLET, ONCE A DAY DURING ONE WEEK | Y | N | 17555 | .5 | DF | TABLET | QD | ||||
125593932 | 12559393 | 3 | SS | SINEMET | CARBIDOPALEVODOPA | 1 | Oral | HALF A TABLET, TWICE A DAY DURING ONE WEEK | Y | N | 17555 | .5 | DF | TABLET | BID | ||||
125593932 | 12559393 | 4 | SS | SINEMET | CARBIDOPALEVODOPA | 1 | Oral | HALF A TABLET, THRICE A DAY. | Y | N | 17555 | .5 | DF | TABLET | TID | ||||
125593932 | 12559393 | 5 | SS | MEMANTINE. | MEMANTINE | 1 | Oral | 1 DF, QD | Y | 0 | 1 | DF | QD | ||||||
125593932 | 12559393 | 6 | C | TAHOR | ATORVASTATIN CALCIUM | 1 | Unknown | UNK | U | 0 | |||||||||
125593932 | 12559393 | 7 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | Unknown | UNK | U | 0 | |||||||||
125593932 | 12559393 | 8 | C | GUTRON | MIDODRINE | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125593932 | 12559393 | 1 | Nervous system disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125593932 | 12559393 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125593932 | 12559393 | Decreased appetite | |
125593932 | 12559393 | Eating disorder | |
125593932 | 12559393 | 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 |
---|---|---|---|---|---|---|
125593932 | 12559393 | 1 | 20160625 | 0 | ||
125593932 | 12559393 | 2 | 2016 | 2016 | 0 | |
125593932 | 12559393 | 3 | 2016 | 2016 | 0 | |
125593932 | 12559393 | 4 | 2016 | 0 | ||
125593932 | 12559393 | 5 | 20160625 | 0 |