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
127272811 12727281 1 I 20160726 20160826 20160909 20160909 EXP GB-MHRA-EYC 00144166 GB-TEVA-689239ACC TEVA 72.00 YR F Y 0.00000 20160909 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
127272811 12727281 1 PS DOXYCYCLINE. DOXYCYCLINE 1 Oral Y U 62421 100 MG
127272811 12727281 2 SS MYSOLINE PRIMIDONE 1 U U 0
127272811 12727281 3 C ALENDRONIC ACID ALENDRONIC ACID 1 0
127272811 12727281 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 0
127272811 12727281 5 C XARELTO RIVAROXABAN 1 0 20 MG
127272811 12727281 6 C VALSARTAN. VALSARTAN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127272811 12727281 1 Lung infection
127272811 12727281 2 Epilepsy

Outcome of event

Event ID CASEID OUTC COD
127272811 12727281 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127272811 12727281 Drug interaction
127272811 12727281 Fatigue
127272811 12727281 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
127272811 12727281 1 20160726 20160728 0