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
126109901 12610990 1 I 20100720 20160727 20160801 20160801 PER US-PFIZER INC-2016365342 PFIZER 57.00 YR F Y 0.00000 20160801 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
126109901 12610990 1 PS BENZONATATE. BENZONATATE 1 UNK U 11210 CAPSULE
126109901 12610990 2 SS ASPIRIN /00002701/ ASPIRIN 1 U 0
126109901 12610990 3 SS TRAZODONE TRAZODONE HYDROCHLORIDE 1 UNK U 0
126109901 12610990 4 SS LEVAQUIN LEVOFLOXACIN 1 UNK U 0
126109901 12610990 5 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK U 0
126109901 12610990 6 SS VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 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
126109901 12610990 Drug hypersensitivity

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

no results found

Therapies reported

no results found