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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4628736 | 4056259 | F | 1 | 4628736-8 | 20030101 | 20050323 | 20050406 | EXP | 03-000513 | WARNER CHILCOTT | F | N | 20050401 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4628736 | 1005852887 | PS | FEMHRT | 1 | ORAL | 5/1000 UG QD, ORAL | U | U | 21065 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4628736 | 1005852887 | NIGHT SWEATS |
Outcome of event
Event ID | OUTC COD |
---|---|
4628736 | HO |
Reactions reported
Event ID | PT |
---|---|
4628736 | CONDITION AGGRAVATED |
4628736 | DIFFICULTY IN WALKING |
4628736 | FIBROMYALGIA |
4628736 | HYPOAESTHESIA |
4628736 | MUSCLE SPASMS |
4628736 | OEDEMA PERIPHERAL |
4628736 | RASH MACULAR |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
4628736 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
4628736 | 1005852887 | 20031001 |