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
126103671 12610367 1 I 201406 20160725 20160801 20160801 EXP JP-GLAXOSMITHKLINE-JP2016JPN107714 GLAXOSMITHKLINE 81.00 YR F Y 39.00000 KG 20160801 CN JP JP

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
126103671 12610367 1 PS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 500 MG, 1D Y 20487 500 MG TABLET QD
126103671 12610367 2 C PREDNISOLONE. PREDNISOLONE 1 5 MG, U 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126103671 12610367 1 Herpes zoster
126103671 12610367 2 Sarcoidosis

Outcome of event

Event ID CASEID OUTC COD
126103671 12610367 OT
126103671 12610367 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126103671 12610367 Altered state of consciousness
126103671 12610367 Depressed level of consciousness
126103671 12610367 Disorientation
126103671 12610367 Dyskinesia
126103671 12610367 Dyslalia
126103671 12610367 Electroencephalogram abnormal
126103671 12610367 Gait disturbance
126103671 12610367 Myoclonus
126103671 12610367 Renal impairment
126103671 12610367 Restlessness
126103671 12610367 Toxic encephalopathy
126103671 12610367 White matter lesion

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
126103671 12610367 1 201406 201406 0