Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107976327 | 10797632 | 7 | F | 2015 | 20160711 | 20150216 | 20160808 | PER | US-PFIZER INC-2015049814 | PFIZER | 74.00 | YR | M | Y | 100.00000 | KG | 20160808 | MD | US | US |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
107976327 | 10797632 | 1 | PS | CADUET | AMLODIPINE BESYLATEATORVASTATIN CALCIUM | 1 | [AMLODIPINE BESILATE 10 MG]/[ATORVASTATIN CALCIUM 80 MG], 1 PILL,ONCE DAILY IN THE MORNING WITH FOOD | Y | U | 0712061 | 21540 | 1 | DF | FILM-COATED TABLET | QD | ||||
107976327 | 10797632 | 2 | SS | CADUET | AMLODIPINE BESYLATEATORVASTATIN CALCIUM | 1 | Y | U | 21540 | FILM-COATED TABLET | |||||||||
107976327 | 10797632 | 3 | C | IBUPROFEN. | IBUPROFEN | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
107976327 | 10797632 | 1 | Hypertension |
107976327 | 10797632 | 2 | Hypercholesterolaemia |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
107976327 | 10797632 | Blood pressure fluctuation | |
107976327 | 10797632 | Dizziness |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
107976327 | 10797632 | 1 | 201501 | 0 |