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
127110351 12711035 1 I 20160726 20160826 20160902 20160902 EXP GB-MHRA-EYC 00144166 GB-MYLANLABS-2016M1036794 MYLAN 0.00 Y 0.00000 20160902 CN GB GB

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
127110351 12711035 1 PS DOXYCYCLINE. DOXYCYCLINE 1 Oral 100 MG, UNK Y U 62337 100 MG
127110351 12711035 2 SS MYSOLINE PRIMIDONE 1 UNK U U 0
127110351 12711035 3 C ALENDRONIC ACID ALENDRONIC ACID 1 UNK U 0
127110351 12711035 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 UNK U 0
127110351 12711035 5 C XARELTO RIVAROXABAN 1 20 MG, UNK U 0 20 MG
127110351 12711035 6 C VALSARTAN. VALSARTAN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127110351 12711035 1 Lung infection
127110351 12711035 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127110351 12711035 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127110351 12711035 Drug interaction
127110351 12711035 Fatigue
127110351 12711035 Headache

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
127110351 12711035 1 20160726 20160728 0