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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124415873 | 12441587 | 3 | F | 20160315 | 20160630 | 20160607 | 20160711 | EXP | PHHY2016FR074896 | SANDOZ | 87.29 | YR | F | Y | 49.00000 | KG | 20160711 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124415873 | 12441587 | 1 | SS | ENTRESTO | SACUBITRILVALSARTAN | 1 | Oral | 2 DF, QD | 130 | DF | Y | 0 | 2 | DF | TABLET | QD | |||
124415873 | 12441587 | 2 | PS | PAROXETINE. | PAROXETINE | 1 | Oral | 20 MG, QD | Y | 75566 | 20 | MG | QD | ||||||
124415873 | 12441587 | 3 | SS | TAHOR | ATORVASTATIN CALCIUM | 1 | Oral | 2 DF, QD | Y | 0 | 2 | DF | QD | ||||||
124415873 | 12441587 | 4 | C | CARDENSIEL | BISOPROLOL FUMARATE | 1 | Unknown | 1.25 MG, QD | U | 0 | 1.25 | MG | QD | ||||||
124415873 | 12441587 | 5 | C | KARDEGIC | ASPIRIN LYSINE | 1 | Unknown | 75 MG, QD | U | 0 | 75 | MG | QD | ||||||
124415873 | 12441587 | 6 | C | DIFFU-K | POTASSIUM CHLORIDE | 1 | Unknown | U | 0 | ||||||||||
124415873 | 12441587 | 7 | C | ZOPICLONE | ZOPICLONE | 1 | Unknown | 3.75 MG, QD | U | 0 | 3.75 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124415873 | 12441587 | 1 | Product used for unknown indication |
124415873 | 12441587 | 2 | Product used for unknown indication |
124415873 | 12441587 | 3 | Product used for unknown indication |
124415873 | 12441587 | 4 | Product used for unknown indication |
124415873 | 12441587 | 5 | Product used for unknown indication |
124415873 | 12441587 | 6 | Product used for unknown indication |
124415873 | 12441587 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124415873 | 12441587 | OT |
124415873 | 12441587 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124415873 | 12441587 | Cardiac failure | |
124415873 | 12441587 | Nausea | |
124415873 | 12441587 | Thrombocytopenia |
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 |
---|---|---|---|---|---|---|
124415873 | 12441587 | 1 | 20160313 | 20160525 | 0 | |
124415873 | 12441587 | 2 | 20160522 | 0 | ||
124415873 | 12441587 | 3 | 20150218 | 20160522 | 0 |