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
125516021 12551602 1 I 20150901 0 20160712 20160712 DIR 67.00 YR F N 85.00000 LBS 20160711 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
125516021 12551602 1 PS LEVAQUIN LEVOFLOXACIN 1 Intravenous (not otherwise specified) N D 0 QD
125516021 12551602 3 C LEVALBUTEROL. LEVALBUTEROL 1 0
125516021 12551602 5 C IPRATROPIUM BROMIDE. IPRATROPIUM BROMIDE 1 0
125516021 12551602 7 C DILT-XR SR 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125516021 12551602 1 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
125516021 12551602 OT
125516021 12551602 HO
125516021 12551602 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125516021 12551602 Activities of daily living impaired
125516021 12551602 Arthralgia
125516021 12551602 Asthenia
125516021 12551602 Exercise tolerance decreased
125516021 12551602 Impaired work ability
125516021 12551602 Pain in extremity
125516021 12551602 Tendon 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
125516021 12551602 1 20150827 20150901 0