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
122392922 12239292 2 F 201601 20160921 20160405 20160928 EXP GB-MHRA-ADR 23399544 GB-MYLANLABS-2016M1013631 MYLAN 0.00 Y 0.00000 20160928 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
122392922 12239292 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK N U 75817

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122392922 12239292 1 Prostatitis

Outcome of event

Event ID CASEID OUTC COD
122392922 12239292 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122392922 12239292 Anxiety
122392922 12239292 Insomnia
122392922 12239292 Muscle spasms
122392922 12239292 Muscle twitching
122392922 12239292 Myalgia
122392922 12239292 Pruritus
122392922 12239292 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
122392922 12239292 1 201601 0