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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4919293 | 5997951 | I | 4919293-7 | 20060101 | 20060207 | 20060216 | EXP | 2006019802 | PFIZER INC | 55 | YR | F | N | 174 | LBS | 20060215 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4919293 | 1006963188 | PS | CELEBREX | 1 | ORAL | 1 IN 1 D), ORAL | D | D | 20998 | ||
4919293 | 1007011228 | C | ZANAFLEX | 1 | |||||||
4919293 | 1007011229 | C | PROTONIX | 1 | |||||||
4919293 | 1007011230 | C | BUSPAR | 1 | |||||||
4919293 | 1007011231 | C | ELAVIL | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4919293 | 1006963188 | FIBROMYALGIA |
4919293 | 1006963188 | OSTEOARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
4919293 | OT |
Reactions reported
Event ID | PT |
---|---|
4919293 | ANXIETY |
4919293 | DEHYDRATION |
4919293 | GASTROOESOPHAGEAL REFLUX DISEASE |
4919293 | ORAL INTAKE REDUCED |
4919293 | STRESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4919293 | CSM |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4919293 | 1006963188 | 20060101 | 20060101 |