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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022551 | 7613048 | I | 7022551-6 | 20100701 | 20100922 | 20100930 | PER | US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2010-BP-10812BP | B.I. PHARMACEUTICALS,INC./RIDGEFIELD | 69 | YR | F | Y | 20100930 | CN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7022551 | 1014810100 | PS | MICARDIS HCT | 1 | ORAL | NOT REPORTED | 021162 | ||||
| 7022551 | 1014810101 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7022551 | 1014810100 | HYPERTENSION |
| 7022551 | 1014810101 | PROPHYLAXIS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 7022551 | DIZZINESS |
| 7022551 | HYPERSOMNIA |
| 7022551 | LOCAL SWELLING |
| 7022551 | MUSCLE TWITCHING |
| 7022551 | OEDEMA PERIPHERAL |
| 7022551 | RED BLOOD CELL SEDIMENTATION RATE INCREASED |
| 7022551 | SKIN DISORDER |
| 7022551 | SUNBURN |
| 7022551 | THYROXINE DECREASED |
| 7022551 | URINARY TRACT INFECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 7022551 | 1014810100 | 20100301 |