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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6259697 | 6985561 | F | 6 | 6259697-6 | 20080911 | 20090618 | 20090701 | EXP | WAES 0904USA01068 | MERCK + CO., INC. | 71 | YR | M | N | 20090630 | MD | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6259697 | 1011852191 | PS | PRINIVIL | 1 | ORAL | 20 MG/DAILY PO | D | D | 19558 | ||
| 6259697 | 1011891273 | SS | FOSINOPRIL SODIUM | 1 | D | D | |||||
| 6259697 | 1011891274 | SS | NEBIVOLOL HCL | 1 | D | D | |||||
| 6259697 | 1011891276 | SS | TORSEMIDE | 1 | D | D | |||||
| 6259697 | 1011891277 | SS | LERCANIDIPINE | 1 | D | D | |||||
| 6259697 | 1011891304 | SS | PLACEBO | 2 | U | U | |||||
| 6259697 | 1011891309 | SS | LISINOPRIL | 1 | ORAL | 20 MG DAILY PO | U | U | |||
| 6259697 | 1011891324 | SS | MIXTARD HUMAN 70/30 | 1 | SUBCUTANEOUS | SC | U | U | |||
| 6259697 | 1011891326 | SS | SAXAGLIPTIN | 2 | ORAL | 2.5 MG PO | |||||
| 6259697 | 1011891327 | SS | DOXAZOSIN MESYLATE | 1 | ORAL | 2 MG DAILY PO | |||||
| 6259697 | 1011891328 | C | NOVAMINSULFON | 2 | |||||||
| 6259697 | 1011891329 | C | TRAMADOL HCL | 1 | |||||||
| 6259697 | 1011891367 | C | AMOXICILLIN AND CLAVULANATE POTSSIUM | 2 | 19558 | ||||||
| 6259697 | 1011891368 | C | ASPIRIN | 1 | 19558 | ||||||
| 6259697 | 1011891370 | C | BISOPROLOL FUMARATE | 1 | |||||||
| 6259697 | 1011891371 | C | CEFUROXIME SODIUM | 1 | |||||||
| 6259697 | 1011891372 | C | METOPROLOL TARTRATE | 1 | |||||||
| 6259697 | 1011891373 | C | TORSEMIDE | 1 | |||||||
| 6259697 | 1011891374 | C | XIPAMIDE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6259697 | 1011891304 | TYPE 2 DIABETES MELLITUS |
| 6259697 | 1011891324 | TYPE 2 DIABETES MELLITUS |
| 6259697 | 1011891326 | DIABETES MELLITUS |
| 6259697 | 1011891327 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6259697 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6259697 | ABDOMINAL PAIN UPPER |
| 6259697 | ARTERIOVENOUS FISTULA THROMBOSIS |
| 6259697 | BLOOD CREATININE INCREASED |
| 6259697 | BLOOD UREA INCREASED |
| 6259697 | LOSS OF CONSCIOUSNESS |
| 6259697 | ORTHOSTATIC HYPOTENSION |
| 6259697 | PLEURAL EFFUSION |
| 6259697 | PNEUMONIA |
| 6259697 | RENAL DISORDER |
| 6259697 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6259697 | FGN |
| 6259697 | HP |
| 6259697 | OTH |
| 6259697 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6259697 | 1011852191 | 20090110 | |||
| 6259697 | 1011891304 | 20090522 | |||
| 6259697 | 1011891309 | 20090110 | |||
| 6259697 | 1011891324 | 20080723 | 20090522 | ||
| 6259697 | 1011891326 | 20070730 | |||
| 6259697 | 1011891327 | 20090114 |