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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124152892 | 12415289 | 2 | F | 20160927 | 20160530 | 20160930 | PER | US-PFIZER INC-2016247629 | PFIZER | 33.00 | YR | F | Y | 86.17000 | KG | 20160930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124152892 | 12415289 | 1 | PS | GENOTROPIN | SOMATROPIN | 1 | Subcutaneous | 0.2 MG, DAILY | U | M11354 | 20280 | .2 | MG | POWDER FOR SOLUTION FOR INJECTION | |||||
124152892 | 12415289 | 2 | SS | GENOTROPIN | SOMATROPIN | 1 | UNK | U | N32312 | 20280 | POWDER FOR SOLUTION FOR INJECTION | ||||||||
124152892 | 12415289 | 3 | SS | GENOTROPIN | SOMATROPIN | 1 | UNK | U | L47974 | 20280 | POWDER FOR SOLUTION FOR INJECTION | ||||||||
124152892 | 12415289 | 4 | C | FISH OIL | FISH OIL | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124152892 | 12415289 | 1 | Hypopituitarism |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124152892 | 12415289 | Energy increased | |
124152892 | 12415289 | Hot flush | |
124152892 | 12415289 | Hyperhidrosis |
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 |
---|---|---|---|---|---|---|
124152892 | 12415289 | 1 | 201603 | 0 |