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
124923232 12492323 2 F 20160302 20160720 20160623 20160729 EXP GB-MHRA-EYC 00140707 GB-TEVA-668581ACC TEVA 33.00 YR M Y 95.25000 KG 20160729 MD 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
124923232 12492323 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 1000 MILLIGRAM DAILY; 22000 MG Y U 74124 500 MG BID
124923232 12492323 2 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK 0 20 MG
124923232 12492323 3 C TAMSULOSIN TAMSULOSIN 1 UNK? 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124923232 12492323 1 Prostatitis
124923232 12492323 2 Anxiety
124923232 12492323 3 Prostatic disorder

Outcome of event

Event ID CASEID OUTC COD
124923232 12492323 OT
124923232 12492323 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124923232 12492323 Depression
124923232 12492323 Dysgeusia
124923232 12492323 Insomnia
124923232 12492323 Joint crepitation
124923232 12492323 Muscle twitching
124923232 12492323 Neuropathy peripheral
124923232 12492323 Photopsia
124923232 12492323 Restlessness
124923232 12492323 Skin burning sensation
124923232 12492323 Suicidal ideation
124923232 12492323 Tendon discomfort
124923232 12492323 Tendon disorder
124923232 12492323 Tendon pain
124923232 12492323 Tinnitus

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
124923232 12492323 1 20160209 20160308 0
124923232 12492323 2 20160204 0
124923232 12492323 3 20160209 20160308 0