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
126729941 12672994 1 I 201511 20160810 20160822 20160822 EXP GB-MHRA-EYC 00143413 GB-BAYER-2016-155636 BAYER 57.00 YR A M Y 79.37000 KG 20160822 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
126729941 12672994 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 200 MG, BID N 19537 200 MG BID
126729941 12672994 2 C LANTUS INSULIN GLARGINE 1 UNK 0
126729941 12672994 3 C NOVORAPID INSULIN ASPART 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126729941 12672994 1 Prostatitis

Outcome of event

Event ID CASEID OUTC COD
126729941 12672994 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126729941 12672994 Arthralgia
126729941 12672994 Depression
126729941 12672994 Epicondylitis
126729941 12672994 Fatigue
126729941 12672994 Musculoskeletal pain
126729941 12672994 Paraesthesia
126729941 12672994 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
126729941 12672994 1 201509 201603 0