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
126805662 12680566 2 F 2016 20160823 20160824 20160902 EXP US-BELCHER PHARMACEUTICALS, LLC-2016VTS00045 BELCHER PHARMACEUTICALS 13.00 YR M Y 61.68000 KG 20160902 CN 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
126805662 12680566 1 PS CEPHALEXIN. CEPHALEXIN 1 Oral 500 MG, 2X/DAY 6363.63623 MG Y U 802J059A 62713 500 MG CAPSULE BID
126805662 12680566 2 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126805662 12680566 1 Mass

Outcome of event

Event ID CASEID OUTC COD
126805662 12680566 OT
126805662 12680566 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126805662 12680566 Abdominal pain upper
126805662 12680566 Chest pain
126805662 12680566 Costochondritis
126805662 12680566 Dyspepsia
126805662 12680566 Hypersensitivity
126805662 12680566 Oesophagitis
126805662 12680566 Weight decreased

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
126805662 12680566 1 201603 201603 0
126805662 12680566 2 2014 0