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
126178611 12617861 1 I 20160719 20160803 20160803 PER US-PFIZER INC-2016353226 PFIZER 0.00 F Y 0.00000 20160803 MD 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
126178611 12617861 1 PS LOPID GEMFIBROZIL 1 UNK U 18422 FILM-COATED TABLET
126178611 12617861 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 77245
126178611 12617861 3 SS ASPIRIN. ASPIRIN 1 UNK U 0
126178611 12617861 4 SS LISINOPRIL. LISINOPRIL 1 UNK U 0
126178611 12617861 5 SS CHOLESTYRAMINE. CHOLESTYRAMINE 1 UNK U 0
126178611 12617861 6 SS GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK U 0
126178611 12617861 7 SS PRAVACHOL PRAVASTATIN SODIUM 1 UNK U 0
126178611 12617861 8 SS SIMVASTATIN. SIMVASTATIN 1 UNK U 0
126178611 12617861 9 SS ASA ASPIRIN 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126178611 12617861 Drug hypersensitivity

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

no results found

Therapies reported

no results found