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
116174762 11617476 2 F 20160802 20151009 20160812 EXP US-BAYER-2015-434327 BAYER 0.00 M Y 86.17000 KG 20160812 OT 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
116174762 11617476 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 750 MG, BID 21473 750 MG MODIFIED-RELEASE FILM-COATED TABLET BID
116174762 11617476 2 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 0 TABLET
116174762 11617476 3 C TESTOSTERONE. TESTOSTERONE 1 ONCE A WEEK 200 MG 7 ML 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116174762 11617476 1 Infected dermal cyst
116174762 11617476 3 Hormone therapy

Outcome of event

Event ID CASEID OUTC COD
116174762 11617476 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116174762 11617476 Depression
116174762 11617476 Emotional distress
116174762 11617476 Injury
116174762 11617476 Neuropathy peripheral
116174762 11617476 Pain
116174762 11617476 Panic attack

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
116174762 11617476 1 20121130 0
116174762 11617476 2 201301 0
116174762 11617476 3 2010 0