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
126587041 12658704 1 I 20150823 0 20160816 20160816 DIR 65.00 YR F N 170.00000 LBS 20160815 N 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
126587041 12658704 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 14 CAPSULE(S) TWICE A DAY TAKEN BY MOUTH N D C602246 20190315 0 14 DF CAPSULE BID
126587041 12658704 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 0
126587041 12658704 5 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
126587041 12658704 7 C SOMA CARISOPRODOL 1 0
126587041 12658704 9 C CLARITIN LORATADINE 1 0
126587041 12658704 11 C VITAMIN B12 CYANOCOBALAMIN 1 0
126587041 12658704 13 C PROBIOTICS PROBIOTICS NOS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126587041 12658704 1 Colitis

Outcome of event

Event ID CASEID OUTC COD
126587041 12658704 DS
126587041 12658704 RI

Reactions reported

Event ID CASEID DRUG REC ACT PT
126587041 12658704 Arthralgia
126587041 12658704 Decreased appetite
126587041 12658704 Depression
126587041 12658704 Fatigue
126587041 12658704 Memory impairment
126587041 12658704 Multiple sclerosis relapse
126587041 12658704 Muscular weakness
126587041 12658704 Pain
126587041 12658704 Pyrexia
126587041 12658704 Rash
126587041 12658704 Rash generalised
126587041 12658704 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
126587041 12658704 1 20150815 20150825 0