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
126439861 12643986 1 I 20160729 20160811 20160811 EXP AU-PFIZER INC-2016378011 PFIZER 0.00 M Y 0.00000 20160811 MD AU AU

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
126439861 12643986 1 PS ATENOLOL. ATENOLOL 1 Oral DOSE UNKNOWN U 73676
126439861 12643986 2 SS ERYTHROMYCIN. ERYTHROMYCIN 1 Unknown DOSE UNKNOWN U 50609
126439861 12643986 3 SS PLENDIL FELODIPINE 1 Oral DOSE UNKNOWN U 0
126439861 12643986 4 SS COLCHICINE. COLCHICINE 1 Unknown DOSE UNKNOWN U 0
126439861 12643986 5 C NILSTAT NYSTATIN 1 Unknown DOSE UNKNOWN 0
126439861 12643986 6 C RANITIDINE. RANITIDINE 1 Unknown DOSE UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126439861 12643986 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126439861 12643986 Hepatitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found