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
127502341 12750234 1 I 20160720 0 20160916 20160916 DIR US-FDA-350756 FDA-CTU 35.00 YR F N 76.50000 KG 20160916 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
127502341 12750234 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N D 0 500 DF BID
127502341 12750234 2 C XANAX ALPRAZOLAM 1 0
127502341 12750234 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127502341 12750234 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
127502341 12750234 OT
127502341 12750234 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127502341 12750234 Contusion
127502341 12750234 Drug hypersensitivity
127502341 12750234 Hypoaesthesia
127502341 12750234 Paraesthesia
127502341 12750234 Skin discolouration
127502341 12750234 Tendonitis

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
127502341 12750234 1 20160720 20160727 0