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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125844562 | 12584456 | 2 | F | 20160621 | 20160808 | 20160722 | 20160818 | PER | US-PFIZER INC-2016317766 | PFIZER | 80.00 | YR | F | Y | 68.00000 | KG | 20160818 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125844562 | 12584456 | 1 | PS | TIKOSYN | DOFETILIDE | 1 | Oral | 500 UG, 2X/DAY EVERY 12 HOURS | N | N45871 | 20931 | 500 | UG | CAPSULE, HARD | BID | ||||
125844562 | 12584456 | 2 | C | PRADAXA | DABIGATRAN ETEXILATE MESYLATE | 1 | 150 MG, UNK [150MG OF 12HR] | 0 | 150 | MG | |||||||||
125844562 | 12584456 | 3 | C | LISINOPRIL. | LISINOPRIL | 1 | 5 MG, DAILY | 0 | 5 | MG | |||||||||
125844562 | 12584456 | 4 | C | MAGNESIUM CHLORIDE. | MAGNESIUM CHLORIDE | 1 | 400 MG, 2X/DAY | 0 | 400 | MG | BID | ||||||||
125844562 | 12584456 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 800 MG, 2X/DAY | 0 | 800 | MG | BID | ||||||||
125844562 | 12584456 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 10 MG, 1X/DAY (BEDTIME) | 0 | 10 | MG | QD | ||||||||
125844562 | 12584456 | 7 | C | PANTOPRAZOLE | PANTOPRAZOLE SODIUM | 1 | 40 MG, DAILY | 0 | 40 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125844562 | 12584456 | 1 | Atrial fibrillation |
125844562 | 12584456 | 2 | Anticoagulant therapy |
125844562 | 12584456 | 4 | Hypomagnesaemia |
125844562 | 12584456 | 5 | Diabetes mellitus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125844562 | 12584456 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125844562 | 12584456 | Activities of daily living impaired | |
125844562 | 12584456 | Condition aggravated | |
125844562 | 12584456 | Decreased appetite | |
125844562 | 12584456 | Dizziness | |
125844562 | 12584456 | Headache | |
125844562 | 12584456 | Hyperhidrosis | |
125844562 | 12584456 | Malaise | |
125844562 | 12584456 | Pain in extremity | |
125844562 | 12584456 | Urinary tract infection |
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 |
---|---|---|---|---|---|---|
125844562 | 12584456 | 1 | 20160616 | 0 |