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
126221301 12622130 1 I 20160225 20160804 20160804 PER US-DRREDDYS-USA/USA/16/0077473 DR REDDYS 0.00 F Y 0.00000 20160804 CN US US

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
126221301 12622130 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral U U UNKNOWN 75593 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126221301 12622130 1 Urinary tract infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126221301 12622130 Dizziness
126221301 12622130 Headache
126221301 12622130 Initial insomnia
126221301 12622130 Pain
126221301 12622130 Tendon pain

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found