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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127458432 | 12745843 | 2 | F | 201609 | 20160921 | 20160915 | 20160930 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201609001667 | ELI LILLY AND CO | 57.92 | YR | F | Y | 0.00000 | 20160930 | CN | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127458432 | 12745843 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Unknown | 1 DF, EACH MORNING | U | U | C530886D | 21318 | 1 | DF | INJECTION | QD | |||
| 127458432 | 12745843 | 2 | C | PYRIDOXAMINE HYDROCHLORIDETHIAMINE HYDROCHLORIDECYANOCOBALAMIN | CYANOCOBALAMINPYRIDOXAMINE HYDROCHLORIDETHIAMINE HYDROCHLORIDE | 1 | UNK, MONTHLY (1/M) | 0 | /month |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127458432 | 12745843 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127458432 | 12745843 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127458432 | 12745843 | Amnesia | |
| 127458432 | 12745843 | Cerebrovascular accident | |
| 127458432 | 12745843 | Drug dose omission | |
| 127458432 | 12745843 | Injection site bruising | |
| 127458432 | 12745843 | Malaise | |
| 127458432 | 12745843 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |