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
126791741 12679174 1 I 201511 20160810 20160824 20160824 EXP GB-AUROBINDO-AUR-APL-2016-10448 AUROBINDO 57.00 YR M Y 79.37000 KG 20160824 CN GB GB

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
126791741 12679174 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 200 MG, TWO TIMES A DAY N U 77859 200 MG BID
126791741 12679174 2 C NOVORAPID INSULIN ASPART 1 Unknown U 0
126791741 12679174 3 C LANTUS INSULIN GLARGINE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126791741 12679174 1 Prostatitis
126791741 12679174 2 Product used for unknown indication
126791741 12679174 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126791741 12679174 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126791741 12679174 Arthralgia
126791741 12679174 Depression
126791741 12679174 Epicondylitis
126791741 12679174 Fatigue
126791741 12679174 Musculoskeletal pain
126791741 12679174 Paraesthesia
126791741 12679174 Tendon pain

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
126791741 12679174 1 201509 201603 0