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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117641403 | 11764140 | 3 | F | 20160724 | 20160728 | 20151120 | 20160826 | PER | US-ELI_LILLY_AND_COMPANY-US201304000578 | ELI LILLY AND CO | 41.94 | YR | F | Y | 0.00000 | 20160826 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117641403 | 11764140 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Unknown | 20 UG, QD | 21318 | 20 | UG | INJECTION | QD | ||||||
117641403 | 11764140 | 2 | SS | FORTEO | TERIPARATIDE | 1 | Unknown | 20 UG, QD | C076729E | 21318 | 20 | UG | INJECTION | QD | |||||
117641403 | 11764140 | 3 | SS | FORTEO | TERIPARATIDE | 1 | Unknown | 20 UG, QD | C465010C | 21318 | 20 | UG | INJECTION | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117641403 | 11764140 | 1 | Osteoporosis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117641403 | 11764140 | Aphonia | |
117641403 | 11764140 | Drug dose omission | |
117641403 | 11764140 | Hypersensitivity | |
117641403 | 11764140 | Lumbar vertebral fracture | |
117641403 | 11764140 | Malaise |
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 |
---|---|---|---|---|---|---|
117641403 | 11764140 | 3 | 201509 | 0 |