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
126585461 12658546 1 I 20151215 20160805 20160817 20160817 EXP GB-MHRA-EYC 00143216 GB-DRREDDYS-GER/UKI/16/0082203 DR REDDYS 69.00 YR M Y 78.00000 KG 20160817 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
126585461 12658546 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral Y U UNKNOWN 75593 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126585461 12658546 1 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126585461 12658546 OT
126585461 12658546 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126585461 12658546 Anxiety
126585461 12658546 Arthralgia
126585461 12658546 Depression
126585461 12658546 Fatigue
126585461 12658546 Heart rate irregular
126585461 12658546 Hypoaesthesia
126585461 12658546 Myalgia
126585461 12658546 Pain
126585461 12658546 Paraesthesia
126585461 12658546 Photophobia
126585461 12658546 Rash
126585461 12658546 Suicidal ideation
126585461 12658546 Tendon disorder

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
126585461 12658546 1 201511 20151123 0