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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5327080 | 6314188 | I | 5327080-3 | 20070510 | 20070517 | EXP | PHBS2007BR08091 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20070517 | MD | BRAZIL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5327080 | 1008487296 | PS | ZOMETA | 1 | 4 MG, UNK | 21223 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5327080 | 1008487296 | MULTIPLE MYELOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
5327080 | OT |
Reactions reported
Event ID | PT |
---|---|
5327080 | OSTEONECROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |