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
116174783 11617478 3 F 20160803 20151009 20160815 EXP US-BAYER-2015-434138 BAYER 0.00 M Y 0.00000 20160815 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
116174783 11617478 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET
116174783 11617478 2 SS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 19537 TABLET
116174783 11617478 3 SS CIPROFLOXACIN. CIPROFLOXACIN 1 500 MG, UNK 0 500 MG
116174783 11617478 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 250 UNK, UNK 0 250 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116174783 11617478 1 Subcutaneous abscess
116174783 11617478 2 Subcutaneous abscess
116174783 11617478 3 Haemorrhoid operation
116174783 11617478 4 Subcutaneous abscess

Outcome of event

Event ID CASEID OUTC COD
116174783 11617478 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116174783 11617478 Cardiovascular disorder
116174783 11617478 Emotional distress
116174783 11617478 Injury
116174783 11617478 Mental disorder
116174783 11617478 Musculoskeletal injury
116174783 11617478 Nervous system disorder
116174783 11617478 Neuropathy peripheral
116174783 11617478 Pain
116174783 11617478 Peripheral nerve injury
116174783 11617478 Skin injury

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
116174783 11617478 1 2000 2004 0
116174783 11617478 2 200504 200703 0
116174783 11617478 3 20050408 20050427 0
116174783 11617478 4 20070131 20070213 0