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
124952302 12495230 2 F 20160302 20160720 20160624 20160804 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-119048 RANBAXY 33.00 YR M Y 95.25000 KG 20160804 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
124952302 12495230 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, BID 22000 MG Y U 75747 500 MG Q12H
124952302 12495230 2 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Unknown 20 MG, UNK U U 0 20 MG
124952302 12495230 3 C TAMSULOSIN TAMSULOSIN 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124952302 12495230 1 Prostatitis
124952302 12495230 2 Anxiety
124952302 12495230 3 Prostatic disorder

Outcome of event

Event ID CASEID OUTC COD
124952302 12495230 LT
124952302 12495230 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124952302 12495230 Depression
124952302 12495230 Dysgeusia
124952302 12495230 Insomnia
124952302 12495230 Joint crepitation
124952302 12495230 Muscle twitching
124952302 12495230 Neuropathy peripheral
124952302 12495230 Photopsia
124952302 12495230 Restlessness
124952302 12495230 Skin burning sensation
124952302 12495230 Suicidal ideation
124952302 12495230 Tendon discomfort
124952302 12495230 Tendon disorder
124952302 12495230 Tendon pain
124952302 12495230 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
124952302 12495230 1 20160209 20160308 0
124952302 12495230 2 20160204 0
124952302 12495230 3 20160209 20160308 0