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
102303743 10230374 3 F 20160721 20140611 20160805 PER US-PFIZER INC-2014159041 PFIZER 49.00 YR F Y 0.00000 20160805 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
102303743 10230374 1 PS CELEBREX CELECOXIB 1 UNK U 20998 CAPSULE, HARD
102303743 10230374 2 SS TRAMADOL. TRAMADOL 1 UNK U 0
102303743 10230374 3 SS VIOXX ROFECOXIB 1 UNK U 0
102303743 10230374 4 SS EMYCIN ERYTHROMYCIN 1 UNK U 0
102303743 10230374 5 SS HYDROCODONE HYDROCODONE 1 UNK U 0
102303743 10230374 6 SS BIAXIN CLARITHROMYCIN 1 UNK U 0
102303743 10230374 7 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK U 0
102303743 10230374 8 SS CRESTOR ROSUVASTATIN CALCIUM 1 UNK U 0
102303743 10230374 9 SS ERMYCIN ERYTHROMYCIN STEARATE 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
102303743 10230374 Drug hypersensitivity

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

no results found

Therapies reported

no results found