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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127867771 | 12786777 | 1 | I | 20160922 | 20160928 | 20160928 | PER | US-PFIZER INC-2016447719 | PFIZER | 71.00 | YR | F | Y | 52.00000 | KG | 20160928 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127867771 | 12786777 | 1 | PS | PROTONIX | PANTOPRAZOLE SODIUM | 1 | UNK | U | 20987 | ||||||||||
127867771 | 12786777 | 2 | SS | ZOFRAN | ONDANSETRON HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
127867771 | 12786777 | 3 | SS | FASLODEX | FULVESTRANT | 1 | Intramuscular | UNK UNK, MONTHLY (1 SYRINGE) | U | 0 | /month |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127867771 | 12786777 | Asthenia | |
127867771 | 12786777 | Feeling abnormal |
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 |
---|---|---|---|---|---|---|
127867771 | 12786777 | 3 | 20150505 | 0 |