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
125865741 12586574 1 I 20160403 0 20160722 20160722 DIR 56.00 YR F N 158.00000 LBS 20160624 N 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
125865741 12586574 1 PS LEVOFLOXACIN. LEVOFLOXACIN 1 Oral 10 PILLS 1 X DAY BY MOUTH N D 0 10 DF QD
125865741 12586574 3 C FLUOXETINE FLUOXETINE HYDROCHLORIDE 1 0
125865741 12586574 4 C SUBOXONE BUPRENORPHINE HYDROCHLORIDENALOXONE HYDROCHLORIDE 1 0
125865741 12586574 6 C ASPRIN ASPIRIN 1 0
125865741 12586574 8 C VITAMIN B12 CYANOCOBALAMIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125865741 12586574 1 Pneumonia

Outcome of event

Event ID CASEID OUTC COD
125865741 12586574 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125865741 12586574 Arthralgia
125865741 12586574 Bone disorder
125865741 12586574 Hypoaesthesia
125865741 12586574 Insomnia
125865741 12586574 Joint stiffness
125865741 12586574 Pain
125865741 12586574 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
125865741 12586574 1 20160330 20160410 0