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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125908351 | 12590835 | 1 | I | 2015 | 20160712 | 20160726 | 20160726 | PER | US-ELI_LILLY_AND_COMPANY-US201607005228 | ELI LILLY AND CO | 0.00 | F | Y | 0.00000 | 20160726 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125908351 | 12590835 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Unknown | UNK | C462926D | 21318 | INJECTION | QD | |||||||
125908351 | 12590835 | 2 | C | MISOPROSTOL. | MISOPROSTOL | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 3 | C | MELOXICAM. | MELOXICAM | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 4 | C | ASPIRIN /00002701/ | ASPIRIN | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 5 | C | HYDROCODONE | HYDROCODONE | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 6 | C | DULOXETINE. | DULOXETINE | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 7 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 8 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 9 | C | PRAVASTATIN. | PRAVASTATIN | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 10 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 11 | C | FLUDROCORTISONE | FLUDROCORTISONE | 1 | UNK | U | 0 | ||||||||||
125908351 | 12590835 | 12 | C | CALCIUM | CALCIUM | 1 | U | 0 | |||||||||||
125908351 | 12590835 | 13 | C | TYLENOL | ACETAMINOPHEN | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125908351 | 12590835 | 1 | Osteoporosis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125908351 | 12590835 | Drug dose omission | |
125908351 | 12590835 | Injection site bruising | |
125908351 | 12590835 | Injection site haemorrhage | |
125908351 | 12590835 | Injection site pain | |
125908351 | 12590835 | Ulcer | |
125908351 | 12590835 | Weight decreased |
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 |
---|---|---|---|---|---|---|
125908351 | 12590835 | 1 | 2015 | 0 |