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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282277 | 6276595 | I | 5282277-6 | 20061001 | 20070320 | 20070331 | EXP | NO-PFIZER INC-2007023091 | PFIZER INC | F | Y | 20070330 | CN | NORWAY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282277 | 1008316801 | PS | PROVERA | 1 | ORAL | 011839 | |||||
| 5282277 | 1008316802 | C | IBUX | 2 | FREQ:AS NEEDED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5282277 | 1008316801 | ENDOMETRIOSIS |
| 5282277 | 1008316802 | TOOTHACHE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282277 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282277 | DISORIENTATION |
| 5282277 | DIZZINESS |
| 5282277 | FEELING ABNORMAL |
| 5282277 | HEADACHE |
| 5282277 | HYPOAESTHESIA |
| 5282277 | MEMORY IMPAIRMENT |
| 5282277 | PHOTOPHOBIA |
| 5282277 | PRESYNCOPE |
| 5282277 | SYNCOPE |
| 5282277 | TRANSIENT ISCHAEMIC ATTACK |
| 5282277 | VISION BLURRED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |