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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124435402 | 12443540 | 2 | F | 20160505 | 20160708 | 20160607 | 20160708 | EXP | CO-PFIZER INC-2016253283 | PFIZER | 14.00 | YR | F | Y | 32.00000 | KG | 20160708 | CN | CO | CO |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124435402 | 12443540 | 1 | PS | GENOTROPIN | SOMATROPIN | 1 | Subcutaneous | 1.2 MG, DAILY | M84765 | 20280 | 1.2 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124435402 | 12443540 | 1 | Growth hormone deficiency |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124435402 | 12443540 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124435402 | 12443540 | Asthenia | |
124435402 | 12443540 | Diarrhoea | |
124435402 | 12443540 | Dizziness | |
124435402 | 12443540 | Gastroenteritis bacterial | |
124435402 | 12443540 | Headache | |
124435402 | 12443540 | Pyrexia | |
124435402 | 12443540 | Vomiting |
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 |
---|---|---|---|---|---|---|
124435402 | 12443540 | 1 | 20160505 | 0 |