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
112056553 11205655 3 F 200509 20160720 20150622 20160803 PER US-BAYER-2015-328326 BAYER 47.31 YR A M Y 171.43000 KG 20160803 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
112056553 11205655 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
112056553 11205655 2 SS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 400 MG, QD 21085 400 MG FILM-COATED TABLET QD
112056553 11205655 3 C COUMADIN WARFARIN SODIUM 1 0
112056553 11205655 4 C LOVENOX ENOXAPARIN SODIUM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112056553 11205655 1 Infection
112056553 11205655 2 Influenza

Outcome of event

Event ID CASEID OUTC COD
112056553 11205655 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112056553 11205655 Activities of daily living impaired
112056553 11205655 Anhedonia
112056553 11205655 Anxiety
112056553 11205655 Burning sensation
112056553 11205655 Discomfort
112056553 11205655 Dysstasia
112056553 11205655 Emotional distress
112056553 11205655 Gait disturbance
112056553 11205655 Hypoaesthesia
112056553 11205655 Injury
112056553 11205655 Muscular weakness
112056553 11205655 Neuropathy peripheral
112056553 11205655 Pain
112056553 11205655 Pain in extremity
112056553 11205655 Paraesthesia

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
112056553 11205655 1 20050815 0
112056553 11205655 2 200509 0