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
127633771 12763377 1 I 20140106 0 20160919 20160919 DIR US-FDA-351041 FDA-CTU 45.00 YR F N 81.00000 KG 20160919 N 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
127633771 12763377 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N Y 0
127633771 12763377 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Oral N D 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127633771 12763377 1 Sinusitis
127633771 12763377 1 Urinary tract infection
127633771 12763377 2 Lymphadenopathy

Outcome of event

Event ID CASEID OUTC COD
127633771 12763377 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127633771 12763377 Anxiety
127633771 12763377 Arthralgia
127633771 12763377 Back pain
127633771 12763377 Depression
127633771 12763377 Dysstasia
127633771 12763377 Fatigue
127633771 12763377 Gait disturbance
127633771 12763377 Impaired work ability
127633771 12763377 Musculoskeletal pain
127633771 12763377 Myalgia
127633771 12763377 Neck pain
127633771 12763377 Pain in extremity
127633771 12763377 Tendon pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found