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
126766871 12676687 1 I 201511 20160810 20160823 20160823 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122408 RANBAXY 57.00 YR M Y 79.37000 KG 20160823 OT 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
126766871 12676687 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 200 MG, BID N U 75747 200 MG Q12H
126766871 12676687 2 C NOVORAPID INSULIN ASPART 1 Unknown U U 0
126766871 12676687 3 C LANTUS INSULIN GLARGINE 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126766871 12676687 1 Prostatitis
126766871 12676687 2 Product used for unknown indication
126766871 12676687 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126766871 12676687 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126766871 12676687 Arthralgia
126766871 12676687 Depression
126766871 12676687 Epicondylitis
126766871 12676687 Fatigue
126766871 12676687 Musculoskeletal pain
126766871 12676687 Paraesthesia
126766871 12676687 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
126766871 12676687 1 201509 201603 0