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
125695171 12569517 1 I 201601 20160708 20160719 20160719 EXP DE-BFARM-16231183 DE-DRREDDYS-GER/GER/16/0081377 DR REDDYS 29.00 YR M Y 82.00000 KG 20160719 CN DE DE

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
125695171 12569517 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral Y U UNKNOWN 75593
125695171 12569517 2 SS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125695171 12569517 1 Bladder discomfort
125695171 12569517 2 Bladder discomfort

Outcome of event

Event ID CASEID OUTC COD
125695171 12569517 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125695171 12569517 Anxiety
125695171 12569517 Arthralgia
125695171 12569517 Cardiovascular disorder
125695171 12569517 Chills
125695171 12569517 Dizziness
125695171 12569517 Feeling cold
125695171 12569517 Gait disturbance
125695171 12569517 Hot flush
125695171 12569517 Joint crepitation
125695171 12569517 Myalgia
125695171 12569517 Palpitations
125695171 12569517 Photophobia
125695171 12569517 Rash
125695171 12569517 Retching
125695171 12569517 Tendonitis
125695171 12569517 Visual impairment
125695171 12569517 Vomiting

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
125695171 12569517 1 201601 0
125695171 12569517 2 201601 0