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
126671691 12667169 1 I 201511 20160810 20160819 20160819 EXP GB-MHRA-EYC 00143413 GB-DRREDDYS-GER/UKI/16/0082353 DR REDDYS 57.00 YR M Y 79.37000 KG 20160819 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
126671691 12667169 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral N U UNKNOWN 75593 200 MG BID
126671691 12667169 2 C NOVORAPID INSULIN ASPART 1 0
126671691 12667169 3 C LANTUS INSULIN GLARGINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126671691 12667169 1 Prostatitis
126671691 12667169 2 Product used for unknown indication
126671691 12667169 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126671691 12667169 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126671691 12667169 Arthralgia
126671691 12667169 Depression
126671691 12667169 Epicondylitis
126671691 12667169 Fatigue
126671691 12667169 Musculoskeletal pain
126671691 12667169 Paraesthesia
126671691 12667169 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
126671691 12667169 1 201509 201603 0