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
127797911 12779791 1 I 20160920 0 20160925 20160925 DIR US-FDA-351488 FDA-CTU 27.00 YR M N 73.35000 KG 20160925 N 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
127797911 12779791 1 PS KEFLEX CEPHALEXIN 1 Oral N D 17163 20170919 0 21 G Q8H
127797911 12779791 3 C MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 0
127797911 12779791 5 C CETIRIZINE HCL CETIRIZINE HYDROCHLORIDE 1 0
127797911 12779791 7 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0
127797911 12779791 9 C PROAIR RESPICLICK ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127797911 12779791 1 Arthropod bite
127797911 12779791 1 Cellulitis

Outcome of event

Event ID CASEID OUTC COD
127797911 12779791 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127797911 12779791 Pain
127797911 12779791 Pruritus
127797911 12779791 Rash generalised
127797911 12779791 Urticaria

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127797911 12779791 1 20160919 20160920 0