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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127414042 | 12741404 | 2 | F | 20160905 | 20160913 | 20160914 | 20160916 | PER | US-PFIZER INC-2016422823 | PFIZER | 56.00 | YR | F | Y | 86.00000 | KG | 20160916 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127414042 | 12741404 | 1 | PS | GENOTROPIN | SOMATROPIN | 1 | 0.8 MG, 1X/DAY | 20280 | .8 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | |||||||
| 127414042 | 12741404 | 2 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 112 MG, 1X/DAY | 0 | 112 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127414042 | 12741404 | 1 | Hypopituitarism |
| 127414042 | 12741404 | 2 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127414042 | 12741404 | Confusional state | |
| 127414042 | 12741404 | Fatigue | |
| 127414042 | 12741404 | Headache | |
| 127414042 | 12741404 | Hypersomnia | |
| 127414042 | 12741404 | Malaise | |
| 127414042 | 12741404 | Panic attack | |
| 127414042 | 12741404 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 127414042 | 12741404 | 1 | 200807 | 0 |