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
124333502 12433350 2 F 200710 20160920 20160603 20160928 PER US-BAYER-2016-101312 BAYER 60.00 YR A M Y 86.17000 KG 20160928 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
124333502 12433350 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 Oral 400 MG, UNK 21085 400 MG FILM-COATED TABLET
124333502 12433350 2 SS LEVAQUIN LEVOFLOXACIN 1 Oral 500 MG, UNK 0 500 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124333502 12433350 1 Plasma cell myeloma
124333502 12433350 2 Plasma cell myeloma

Outcome of event

Event ID CASEID OUTC COD
124333502 12433350 HO
124333502 12433350 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124333502 12433350 Asthenia
124333502 12433350 Burning sensation
124333502 12433350 Cardiovascular disorder
124333502 12433350 Hypoaesthesia
124333502 12433350 Mental disorder
124333502 12433350 Musculoskeletal injury
124333502 12433350 Nervous system disorder
124333502 12433350 Neuropathy peripheral
124333502 12433350 Pain
124333502 12433350 Paraesthesia
124333502 12433350 Sensory disturbance
124333502 12433350 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
124333502 12433350 1 20110511 0
124333502 12433350 2 20071001 0