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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4718694 | 4162594 | F | 7 | 4718694-X | 20040603 | 20050712 | 20050719 | EXP | 200418321BWH | BAYER PHARMACEUTICALS CORPORATION | 48 | YR | M | N | 20050718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4718694 | 1006224717 | PS | LEVITRA | 1 | ORAL | SEE IMAGE | D | D | 21400 | ||
| 4718694 | 1006254968 | C | COCAINE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4718694 | 1006224717 | ERECTILE DYSFUNCTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4718694 | HO |
| 4718694 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 4718694 | ARRHYTHMIA |
| 4718694 | ATRIOVENTRICULAR BLOCK |
| 4718694 | BLOOD POTASSIUM DECREASED |
| 4718694 | BLOOD PRESSURE SYSTOLIC INCREASED |
| 4718694 | BRADYCARDIA |
| 4718694 | CHEST PAIN |
| 4718694 | DIZZINESS |
| 4718694 | DRUG ABUSER |
| 4718694 | ELECTROCARDIOGRAM T WAVE INVERSION |
| 4718694 | HAEMATOCRIT DECREASED |
| 4718694 | HAEMOGLOBIN DECREASED |
| 4718694 | PALPITATIONS |
| 4718694 | RED BLOOD CELL COUNT DECREASED |
| 4718694 | RESPIRATORY RATE INCREASED |
| 4718694 | SYNCOPE |
| 4718694 | VENTRICULAR HYPERTROPHY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4718694 | CR |
| 4718694 | CSM |
| 4718694 | HP |
| 4718694 | OTH |
Therapies reported
| no results found |