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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331392 | 4122234 | I | 4331392-X | 20040318 | 20040331 | EXP | 2004018949 | WWS PFIZER INC. | 67 | YR | M | N | 20040330 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4331392 | 1004759746 | PS | NIFEDIPINE | 1 | U | U | 18482 | ||||
| 4331392 | 1004772688 | SS | DILTIAZEM | 1 | U | U |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4331392 | 1004759746 | HYPERTENSION |
| 4331392 | 1004772688 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4331392 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4331392 | BLOOD CREATINE PHOSPHOKINASE INCREASED |
| 4331392 | BLOOD MAGNESIUM INCREASED |
| 4331392 | BLOOD PRESSURE DECREASED |
| 4331392 | BUNDLE BRANCH BLOCK RIGHT |
| 4331392 | CARDIAC ARREST |
| 4331392 | CARDIOGENIC SHOCK |
| 4331392 | DRUG INEFFECTIVE |
| 4331392 | ELECTROCARDIOGRAM T WAVE INVERSION |
| 4331392 | HEART INJURY |
| 4331392 | SOMNOLENCE |
| 4331392 | VENTRICULAR DYSKINESIA |
| 4331392 | VENTRICULAR HYPOKINESIA |
| 4331392 | VENTRICULAR TACHYCARDIA |
| 4331392 | WHITE BLOOD CELL COUNT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4331392 | FGN |
| 4331392 | HP |
| 4331392 | LIT |
Therapies reported
| no results found |