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
125632411 12563241 1 I 201606 20160712 20160715 20160715 PER US-009507513-1607USA005624 MERCK 60.12 YR M Y 95.20000 KG 20160715 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
125632411 12563241 1 PS ZEPATIER ELBASVIRGRAZOPREVIR 1 Oral UNK 208261 TABLET
125632411 12563241 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 0 10 MG TABLET BID
125632411 12563241 3 SS AUBAGIO TERIFLUNOMIDE 1 Oral UNK 0
125632411 12563241 4 SS TYSABRI NATALIZUMAB 1 U 0
125632411 12563241 5 C TOPROL XL METOPROLOL SUCCINATE 1 U 0
125632411 12563241 6 C CELEXA CITALOPRAM HYDROBROMIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125632411 12563241 1 Hepatitis C
125632411 12563241 2 Gait disturbance
125632411 12563241 3 Multiple sclerosis
125632411 12563241 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125632411 12563241 Confusional state
125632411 12563241 Dizziness
125632411 12563241 Dysgeusia
125632411 12563241 Memory impairment
125632411 12563241 Nausea
125632411 12563241 Thinking abnormal

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
125632411 12563241 1 20160617 0
125632411 12563241 2 20110214 0