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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6082879 | 6912893 | I | 6082879-3 | 20090210 | 20090218 | EXP | PHEH2009US01592 | NOVARTIS PHARMACEUTICALS CORP. | F | Y | 20090218 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6082879 | 1011146564 | PS | RECLAST | 1 | UNK | 021817 | |||||
| 6082879 | 1011146565 | SS | ARTHROTEC | 1 | ORAL | 50 MG, BID | |||||
| 6082879 | 1011146566 | SS | ARTHROTEC | 1 | ORAL | 50 MG, QD | |||||
| 6082879 | 1011146567 | C | PLAVIX | 1 | 75 MG, QD |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6082879 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6082879 | HAEMORRHAGE |
| 6082879 | 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 |
|---|---|---|---|---|---|
| 6082879 | 1011146564 | 20080301 |