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
118894022 11889402 2 F 20160810 20160105 20160815 PER US-PFIZER INC-2015477723 PFIZER 67.00 YR M Y 0.00000 20160815 CN 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
118894022 11889402 1 PS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 UNK U 20702
118894022 11889402 2 SS GLIPIZIDE. GLIPIZIDE 1 UNK U 17783
118894022 11889402 3 SS ASPIRIN /00002701/ ASPIRIN 1 81 MG, 1X/DAY (AT BREAKFAST) 0 81 MG QD
118894022 11889402 4 SS METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U 0
118894022 11889402 5 SS ISOSORBID MONONITRATE ISOSORBIDE MONONITRATE 1 UNK U 0
118894022 11889402 6 SS CLONAZEPAM. CLONAZEPAM 1 UNK U 0
118894022 11889402 7 SS LEVEMIR INSULIN DETEMIR 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118894022 11889402 5 Cardiac disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118894022 11889402 Drug hypersensitivity

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

no results found

Therapies reported

no results found