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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6668400 | 7678128 | I | 6668400-7 | 20100324 | 20100406 | EXP | PHHY2010BR19211 | NOVARTIS PHARMACEUTICAL CORPORATION | YR | F | Y | 20100406 | CN | BRAZIL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6668400 | 1013448471 | PS | AMLODIPINE BESYLATE AND VALSARTAN | 1 | 80/5 MG, (2 TABLETS,DAILY) | 21990 | |||||
6668400 | 1013448472 | SS | EXFORGE | 1 | 80/5 MG (1 TABLET, DAILY) | 021990 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6668400 | OT |
Reactions reported
Event ID | PT |
---|---|
6668400 | BLOOD PRESSURE FLUCTUATION |
6668400 | CONFUSIONAL STATE |
6668400 | DRUG DISPENSING ERROR |
6668400 | LIMB INJURY |
6668400 | MALAISE |
6668400 | WRONG TECHNIQUE IN DRUG USAGE PROCESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |