Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6819759 | 7391397 | F | 6819759-9 | 20090930 | 20100621 | 20100707 | EXP | PHHY2010CA29646 | NOVARTIS PHARMACEUTICAL CORPORATION | 80 | YR | F | Y | 20100707 | MD | CANADA |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
6819759 | 1014047070 | PS | ZOLEDRONIC | 1 | INTRAVENOUS | 5 MG | 21817 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6819759 | 1014047070 | OSTEOPOROSIS |
Outcome of event
Event ID | OUTC COD |
---|---|
6819759 | HO |
6819759 | OT |
Reactions reported
Event ID | PT |
---|---|
6819759 | HIP ARTHROPLASTY |
6819759 | HIP FRACTURE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6819759 | 1014047070 | 20090629 |