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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6451437 | 7185181 | F | 6451437-0 | 20090105 | 20091123 | PER | US-BRISTOL-MYERS SQUIBB COMPANY-14390272 | BRISTOL-MYERS SQUIBB COMPANY | 90 | YR | F | Y | 59 | KG | 20091123 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6451437 | 1012627360 | PS | AVALIDE | 1 | INITIALLY 150MG AND INCREASED TO 1 DF- 300MG/12.5MG; LOT #: 6H2152A. EXPIRATION DATE: 08/2009. | 8B2016A | 020758 | ||||
| 6451437 | 1012627361 | C | ACIPHEX | 1 | |||||||
| 6451437 | 1012627362 | C | LUNESTA | 1 | |||||||
| 6451437 | 1012627363 | C | ATENOLOL | 1 | |||||||
| 6451437 | 1012627364 | C | HYDROCODONE | 2 | |||||||
| 6451437 | 1012627365 | C | AMLODIPINE BESYLATE+BENAZEPRIL HCL | 2 | 10MG/20MG |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6451437 | BLOOD PRESSURE INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |