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
126759231 12675923 1 I 20070503 0 20160822 20160822 DIR 28.00 YR M N 145.00000 LBS 20160819 N COUNTRY NOT SPECIFIED

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
126759231 12675923 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126759231 12675923 1 Eye infection
126759231 12675923 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126759231 12675923 DS
126759231 12675923 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126759231 12675923 Back pain
126759231 12675923 Bone disorder
126759231 12675923 Bursitis
126759231 12675923 Disturbance in attention
126759231 12675923 Epistaxis
126759231 12675923 Erectile dysfunction
126759231 12675923 Exostosis
126759231 12675923 Genital disorder male
126759231 12675923 Hallucination
126759231 12675923 Hypoaesthesia
126759231 12675923 Impaired work ability
126759231 12675923 Male genital atrophy
126759231 12675923 Muscle atrophy
126759231 12675923 Muscular weakness
126759231 12675923 Musculoskeletal pain
126759231 12675923 Paraesthesia
126759231 12675923 Skin burning sensation
126759231 12675923 Tendon disorder
126759231 12675923 Tendon rupture
126759231 12675923 Tendonitis
126759231 12675923 Thrombocytopenia
126759231 12675923 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
126759231 12675923 1 20070503 20071201 0