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
126770261 12677026 1 I 201511 20160810 20160823 20160823 EXP GB-MHRA-EYC 00143413 GB-TEVA-684908ACC TEVA 57.00 YR M Y 79.37000 KG 20160823 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
126770261 12677026 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 400 MILLIGRAM DAILY; N U 74124 200 MG BID
126770261 12677026 2 C NOVORAPID INSULIN ASPART 1 0
126770261 12677026 3 C LANTUS INSULIN GLARGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126770261 12677026 1 Prostatitis

Outcome of event

Event ID CASEID OUTC COD
126770261 12677026 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126770261 12677026 Arthralgia
126770261 12677026 Depression
126770261 12677026 Epicondylitis
126770261 12677026 Fatigue
126770261 12677026 Musculoskeletal pain
126770261 12677026 Paraesthesia
126770261 12677026 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
126770261 12677026 1 201509 201603 0