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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125447383 | 12544738 | 3 | F | 20160729 | 20160711 | 20160819 | PER | US-PFIZER INC-2016323099 | PFIZER | 7.00 | YR | M | Y | 0.00000 | 20160819 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125447383 | 12544738 | 1 | PS | GENOTROPIN | SOMATROPIN | 1 | Subcutaneous | 0.6 MG, 1X/DAY | 20280 | .6 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | ||||||
| 125447383 | 12544738 | 2 | SS | GENOTROPIN | SOMATROPIN | 1 | Subcutaneous | 0.8 MG, 1X/DAY (0.8 MG, SUB-Q AT BEDTIME) | 20280 | .8 | MG | POWDER FOR SOLUTION FOR INJECTION | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125447383 | 12544738 | 1 | Growth hormone deficiency |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125447383 | 12544738 | Arthropathy | |
| 125447383 | 12544738 | Gait disturbance | |
| 125447383 | 12544738 | Headache | |
| 125447383 | 12544738 | Myalgia | |
| 125447383 | 12544738 | Pain in extremity |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |