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
111682423 11168242 3 F 20160811 20150605 20160817 PER US-BAYER-2015-291414 BAYER 0.00 F Y 0.00000 20160817 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
111682423 11168242 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, UNK 21085 400 MG FILM-COATED TABLET
111682423 11168242 2 C PROVENTIL ALBUTEROL 1 UNK 0
111682423 11168242 3 C AUGMENTIN AMOXICILLINCLAVULANATE POTASSIUM 1 Oral 875- 125 MG PER TABLET, BID 0 BID
111682423 11168242 4 C PREDNISONE. PREDNISONE 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
111682423 11168242 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111682423 11168242 Anxiety
111682423 11168242 Emotional distress
111682423 11168242 Feeling abnormal
111682423 11168242 Injury
111682423 11168242 Neuropathy peripheral
111682423 11168242 Pain

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
111682423 11168242 1 20120503 20120509 0
111682423 11168242 3 20120508 20120515 0