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
126337921 12633792 1 I 20160729 20160809 20160809 EXP AU-PFIZER INC-2016376820 PFIZER 0.00 M Y 0.00000 20160809 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
126337921 12633792 1 PS ATENOLOL. ATENOLOL 1 Unknown UNK U 73676
126337921 12633792 2 SS ALLOPURINOL. ALLOPURINOL 1 Unknown UNK U 0
126337921 12633792 3 SS CHLOROTHIAZIDE. CHLOROTHIAZIDE 1 Unknown UNK U 0
126337921 12633792 4 SS COLCHICINE. COLCHICINE 1 Unknown UNK U 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126337921 12633792 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126337921 12633792 Hepatitis
126337921 12633792 Neuritis
126337921 12633792 Neutropenia
126337921 12633792 Thrombocytopenia
126337921 12633792 Vomiting

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

no results found

Therapies reported

no results found