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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118796853 | 11879685 | 3 | F | 201506 | 20160713 | 20151230 | 20160724 | EXP | BR-ELI_LILLY_AND_COMPANY-BR201512007214 | ELI LILLY AND CO | 74.69 | YR | F | Y | 63.00000 | KG | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 118796853 | 11879685 | 1 | PS | FORTEO | TERIPARATIDE | 1 | Subcutaneous | UNK, UNKNOWN | N | C453946 | 21318 | INJECTION | |||||||
| 118796853 | 11879685 | 2 | SS | FORTEO | TERIPARATIDE | 1 | Subcutaneous | UNK, QD | N | 21318 | INJECTION | QD | |||||||
| 118796853 | 11879685 | 3 | C | DIOVAN | VALSARTAN | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 118796853 | 11879685 | 4 | C | ANADOR /00015901/ | 2 | Unknown | UNK, UNKNOWN | U | 0 | ||||||||||
| 118796853 | 11879685 | 5 | C | NIMESULIDA | NIMESULIDE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 118796853 | 11879685 | 6 | C | PYRIDOXAMINE HYDROCHLORIDETHIAMINE HYDROCHLORIDECYANOCOBALAMIN | CYANOCOBALAMINPYRIDOXAMINE HYDROCHLORIDETHIAMINE HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | 0 | ||||||||||
| 118796853 | 11879685 | 7 | C | VITAMIN D /00107901/ | ERGOCALCIFEROL | 1 | Unknown | UNK, UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 118796853 | 11879685 | 1 | Osteoporosis |
| 118796853 | 11879685 | 3 | Hypertension |
| 118796853 | 11879685 | 4 | Inflammation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 118796853 | 11879685 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 118796853 | 11879685 | Arthralgia | |
| 118796853 | 11879685 | Blood uric acid increased | |
| 118796853 | 11879685 | Disorientation | |
| 118796853 | 11879685 | Dizziness | |
| 118796853 | 11879685 | Drug dose omission | |
| 118796853 | 11879685 | Drug ineffective | |
| 118796853 | 11879685 | Erythema | |
| 118796853 | 11879685 | Fall | |
| 118796853 | 11879685 | Hypersensitivity | |
| 118796853 | 11879685 | Injection site erythema | |
| 118796853 | 11879685 | Injection site pain | |
| 118796853 | 11879685 | Joint swelling | |
| 118796853 | 11879685 | Malaise | |
| 118796853 | 11879685 | Myocardial infarction | |
| 118796853 | 11879685 | Pain | |
| 118796853 | 11879685 | Peripheral swelling | |
| 118796853 | 11879685 | Tachycardia | |
| 118796853 | 11879685 | Varicose vein | |
| 118796853 | 11879685 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 118796853 | 11879685 | 1 | 201506 | 0 | ||
| 118796853 | 11879685 | 3 | 2014 | 0 |