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
126062981 12606298 1 I 20160709 0 20160728 20160728 DIR 77.00 YR F N 170.00000 LBS 20160727 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
126062981 12606298 1 PS FLAGYL METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE 1 Oral Y D 0 1 DF COATED TABLET Q6H
126062981 12606298 3 C SULFASALZINE SULFASALAZINE 1 0
126062981 12606298 5 C POTASSIUM SUPPLEMENTS 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126062981 12606298 1 Gastrointestinal infection

Outcome of event

Event ID CASEID OUTC COD
126062981 12606298 LT
126062981 12606298 DS
126062981 12606298 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126062981 12606298 Amnesia
126062981 12606298 Asthenia
126062981 12606298 Confusional state
126062981 12606298 Crohn's disease
126062981 12606298 Hallucination
126062981 12606298 Motor dysfunction
126062981 12606298 Musculoskeletal stiffness
126062981 12606298 Pain
126062981 12606298 Rectal haemorrhage
126062981 12606298 Speech disorder

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
126062981 12606298 1 20160706 20160713 0