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
120513012 12051301 2 F 20160908 20160209 20160909 PER US-PFIZER INC-2016071872 PFIZER 53.00 YR F Y 0.00000 20160909 OT 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
120513012 12051301 1 SS AMOXICILLIN. AMOXICILLIN 1 UNK U 0
120513012 12051301 2 PS AMPICILLIN SODIUM. AMPICILLIN SODIUM 1 UNK U 202864
120513012 12051301 3 SS ENBREL ETANERCEPT 1 UNK U 0
120513012 12051301 4 SS FENTANYL CITRATE. FENTANYL CITRATE 1 UNK U 19115
120513012 12051301 5 SS MORPHINE SULFATE. MORPHINE SULFATE 1 UNK U 19999
120513012 12051301 6 SS HUMIRA ADALIMUMAB 1 UNK U 0
120513012 12051301 7 SS REMICADE INFLIXIMAB 1 UNK U 0
120513012 12051301 8 SS SEROQUEL QUETIAPINE FUMARATE 1 UNK U 0
120513012 12051301 9 SS PAXIL PAROXETINE HYDROCHLORIDE 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
120513012 12051301 Drug hypersensitivity

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

no results found

Therapies reported

no results found