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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6809879 | 7448692 | I | 6809879-7 | 20100618 | 20100630 | EXP | US-WATSON-2010-08566 | WATSON | 63 | YR | F | Y | 20100630 | OT | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6809879 | 1014005280 | PS | ALENDRONATE SODIUM | 1 | UNK | UNCONFIRMED | 076984 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6809879 | 1014005280 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
Event ID | OUTC COD |
---|---|
6809879 | HO |
Reactions reported
Event ID | PT |
---|---|
6809879 | FEMUR 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 |
---|---|---|---|---|---|
6809879 | 1014005280 | 1460 | DAY |