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
125948371 12594837 1 I 20160714 20160726 20160726 EXP DE-BFARM-16238379 DE-TEVA-677523GER TEVA 0.00 F Y 0.00000 20160726 CN DE DE

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
125948371 12594837 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 U 74124

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125948371 12594837 1 Pyelonephritis

Outcome of event

Event ID CASEID OUTC COD
125948371 12594837 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125948371 12594837 Affect lability
125948371 12594837 Alopecia
125948371 12594837 Bronchitis
125948371 12594837 Chest discomfort
125948371 12594837 Cognitive disorder
125948371 12594837 Fatigue
125948371 12594837 Fungal infection
125948371 12594837 Headache
125948371 12594837 Immune system disorder
125948371 12594837 Muscular weakness
125948371 12594837 Musculoskeletal discomfort
125948371 12594837 Onychoclasis
125948371 12594837 Oropharyngeal pain
125948371 12594837 Tendon discomfort
125948371 12594837 Vulvovaginal candidiasis
125948371 12594837 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
125948371 12594837 1 201507 0