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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125560041 | 12556004 | 1 | I | 20160610 | 0 | 20160713 | 20160713 | DIR | 78.00 | YR | F | N | 109.00000 | LBS | 20160712 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125560041 | 12556004 | 1 | PS | RECLAST | ZOLEDRONIC ACID | 1 | 0 | ||||||||||||
| 125560041 | 12556004 | 2 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
| 125560041 | 12556004 | 4 | C | LETROZOLE. | LETROZOLE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125560041 | 12556004 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125560041 | 12556004 | DS |
| 125560041 | 12556004 | HO |
| 125560041 | 12556004 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125560041 | 12556004 | Atrial fibrillation | |
| 125560041 | 12556004 | Cardiac arrest | |
| 125560041 | 12556004 | Loss of consciousness | |
| 125560041 | 12556004 | Pain | |
| 125560041 | 12556004 | Syncope | |
| 125560041 | 12556004 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |