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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6386378 | 7143962 | I | 6386378-0 | 20060601 | 20090930 | DIR | 58 | F | N | 135 | LBS | 20090929 | CN | N | Y | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6386378 | 1012369905 | PS | ACTONEL | 1 | ORAL | ONE TABLET WEEKLY PO (THERAPY DATES BEST ESTIMATE) | D | D | 20091230 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6386378 | 1012369905 | OSTEOPOROSIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6386378 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6386378 | ARTHRALGIA |
| 6386378 | BACK PAIN |
| 6386378 | MIDDLE INSOMNIA |
| 6386378 | MUSCULOSKELETAL PAIN |
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 |
|---|---|---|---|---|---|
| 6386378 | 1012369905 | 20050719 | 20090920 |