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
127801842 12780184 2 F 20141107 20160927 20160926 20160927 EXP ES-AGEMED-943127440 ES-PFIZER INC-2016441168 PFIZER 86.00 YR M Y 0.00000 20160927 MD ES ES

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
127801842 12780184 1 PS ALDACTONE SPIRONOLACTONE 1 Oral Y 12151 FILM-COATED TABLET
127801842 12780184 2 I SINTROM ACENOCOUMAROL 1 Oral Y 0
127801842 12780184 3 I NORFLOXACIN NORFLOXACIN 1 Oral 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127801842 12780184 1 Chronic kidney disease
127801842 12780184 2 Atrial fibrillation
127801842 12780184 3 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
127801842 12780184 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127801842 12780184 Coagulopathy
127801842 12780184 Drug interaction
127801842 12780184 Hyperkalaemia

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
127801842 12780184 1 20141022 20141107 0
127801842 12780184 2 20141107 0
127801842 12780184 3 20141018 0