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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126978851 | 12697885 | 1 | I | 201607 | 20160822 | 20160830 | 20160830 | PER | US-PFIZER INC-2016398721 | PFIZER | 7.00 | YR | M | Y | 23.00000 | KG | 20160830 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126978851 | 12697885 | 1 | PS | GENOTROPIN | SOMATROPIN | 1 | Subcutaneous | 1 MG, 1X/DAY, BEFORE BEDTIME NIGHTLY | U | M63189 | 20280 | 1 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | ||||
126978851 | 12697885 | 2 | SS | GENOTROPIN | SOMATROPIN | 1 | U | 20280 | POWDER FOR SOLUTION FOR INJECTION | ||||||||||
126978851 | 12697885 | 3 | SS | GENOTROPIN | SOMATROPIN | 1 | U | 20280 | POWDER FOR SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126978851 | 12697885 | 1 | Dwarfism |
126978851 | 12697885 | 2 | Body height below normal |
126978851 | 12697885 | 3 | Hypopituitarism |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126978851 | 12697885 | Headache |
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 |
---|---|---|---|---|---|---|
126978851 | 12697885 | 1 | 20131210 | 0 |