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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5040495 | 6045522 | F | 5040495-6 | 20060301 | 20060502 | 20060630 | EXP | US-ROCHE-446548 | ROCHE | 72 | YR | F | Y | 20060630 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5040495 | 1007431408 | PS | BONIVA | 1 | ORAL | 21455 | |||||
5040495 | 1007431409 | C | VITAMINS NOS | 2 | ORAL | ||||||
5040495 | 1007431410 | C | ZYRTEC | 1 | ORAL | ||||||
5040495 | 1007431411 | C | SINGULAIR | 1 | ORAL | ||||||
5040495 | 1007431412 | C | PRILOSEC | 1 | |||||||
5040495 | 1007431413 | C | LIPITOR | 1 | |||||||
5040495 | 1007431414 | C | CLARINEX | 1 | |||||||
5040495 | 1007431415 | C | ASPIRIN | 1 | |||||||
5040495 | 1007431416 | C | CELEBREX | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5040495 | 1007431408 | OSTEOPOROSIS |
5040495 | 1007431410 | ASTHMA |
5040495 | 1007431411 | ASTHMA |
5040495 | 1007431416 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5040495 | OT |
Reactions reported
Event ID | PT |
---|---|
5040495 | ARTHRALGIA |
5040495 | CARPAL TUNNEL SYNDROME |
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 |
---|---|---|---|---|---|
5040495 | 1007431408 | 20060301 | 20060401 | 32 | DAY |
5040495 | 1007431416 | 19960615 |