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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126937001 | 12693700 | 1 | I | 20160804 | 20160809 | 20160829 | 20160829 | PER | US-PFIZER INC-2016381752 | PFIZER | 72.00 | YR | M | Y | 91.00000 | KG | 20160829 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126937001 | 12693700 | 1 | PS | TIKOSYN | DOFETILIDE | 1 | Oral | 250 UG, 2X/DAY (EVERY 12 HOURS ) | 20931 | 250 | UG | CAPSULE, HARD | BID | ||||||
126937001 | 12693700 | 2 | SS | DOFETILIDE. | DOFETILIDE | 1 | Oral | 250 UG, 2X/DAY (EVERY 12 HOURS) | 0 | 250 | UG | CAPSULE | BID | ||||||
126937001 | 12693700 | 3 | C | LOSARTAN. | LOSARTAN | 1 | 25 MG, 2X/DAY (50MG TABLET HALF TABLET IN MORNING AND HALF AT NIGHT) | 0 | 25 | MG | TABLET | BID | |||||||
126937001 | 12693700 | 4 | C | WARFARIN | WARFARIN | 1 | 7.5MG ON MON, WED, FRI; 5MG THE REST OF WEEK IN MORNING | 0 | |||||||||||
126937001 | 12693700 | 5 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 40 MG, 1X/DAY (IN MORNING AND BEFORE DINNER) | 0 | 40 | MG | QD | ||||||||
126937001 | 12693700 | 6 | C | IRON | IRON | 1 | TAKES IN MORNING | 0 | |||||||||||
126937001 | 12693700 | 7 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 40 MG, IN THE EVNEING | 0 | 40 | MG | |||||||||
126937001 | 12693700 | 8 | C | RANITIDINE. | RANITIDINE | 1 | 150 MG, IN THE EVENING | 0 | 150 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126937001 | 12693700 | 1 | Atrial fibrillation |
126937001 | 12693700 | 2 | Atrial fibrillation |
126937001 | 12693700 | 4 | Blood disorder |
126937001 | 12693700 | 5 | Gastrooesophageal reflux disease |
126937001 | 12693700 | 6 | Mineral supplementation |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126937001 | 12693700 | Drug dispensing error | |
126937001 | 12693700 | Drug ineffective |
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 |
---|---|---|---|---|---|---|
126937001 | 12693700 | 1 | 2014 | 0 | ||
126937001 | 12693700 | 2 | 201607 | 0 |