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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123170933 | 12317093 | 3 | F | 2014 | 20160810 | 20160429 | 20160812 | EXP | US-ELI_LILLY_AND_COMPANY-US201601002668 | ELI LILLY AND CO | 61.36 | YR | M | Y | 111.00000 | KG | 20160812 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123170933 | 12317093 | 1 | PS | AXIRON | TESTOSTERONE | 1 | Unknown | UNK, UNKNOWN | 22504 | ORAL LIQUID | |||||||||
| 123170933 | 12317093 | 2 | SS | TESTOSTERONE. | TESTOSTERONE | 1 | Unknown | UNK, UNKNOWN | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123170933 | 12317093 | 1 | Blood testosterone decreased |
| 123170933 | 12317093 | 2 | Blood testosterone decreased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123170933 | 12317093 | OT |
| 123170933 | 12317093 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123170933 | 12317093 | Atrial fibrillation | |
| 123170933 | 12317093 | Thrombosis |
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 |
|---|---|---|---|---|---|---|
| 123170933 | 12317093 | 1 | 2012 | 2013 | 0 | |
| 123170933 | 12317093 | 2 | 20120308 | 0 |