The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
125413032 12541303 2 F 20160323 20160701 20160708 20160712 EXP FR-PFIZER INC-2016327907 PFIZER 76.00 YR M Y 82.00000 KG 20160712 OT FR FR

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
125413032 12541303 1 PS ALDACTONE SPIRONOLACTONE 1 Oral 75 MG, 1X/DAY Y 12151 75 MG FILM-COATED TABLET QD
125413032 12541303 2 SS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral 200 MG, 1X/DAY Y N 18972 200 MG TABLET QD
125413032 12541303 3 SS ATENOLOL. ATENOLOL 1 Oral 200 MG, 1X/DAY Y 73676 200 MG TABLET QD
125413032 12541303 4 C KARDEGIC ASPIRIN LYSINE 1 0
125413032 12541303 5 C TAHOR ATORVASTATIN CALCIUM 1 0
125413032 12541303 6 C PLAVIX CLOPIDOGREL BISULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125413032 12541303 1 Hypertension
125413032 12541303 2 Atrial fibrillation
125413032 12541303 3 Myocardial ischaemia

Outcome of event

Event ID CASEID OUTC COD
125413032 12541303 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125413032 12541303 Blood pressure decreased
125413032 12541303 Bradycardia
125413032 12541303 Hyperkalaemia
125413032 12541303 Sinoatrial block

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
125413032 12541303 1 20160326 0
125413032 12541303 2 20160326 0
125413032 12541303 3 20160326 0