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
126683671 12668367 1 I 2001 20151105 20160819 20160819 EXP US-PRESTIUM-2015RN000209 RENAISSANCE 0.00 Y 0.00000 20160819 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
126683671 12668367 1 PS ACYCLOVIR. ACYCLOVIR 1 Oral 500 MG U UNKNOWN 20089 500 MG TABLET
126683671 12668367 2 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 1 G, 1 D Y 0 1 G TABLET
126683671 12668367 3 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Y 0 TABLET
126683671 12668367 4 C PHENOBARBITAL. PHENOBARBITAL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126683671 12668367 1 Oral herpes
126683671 12668367 2 Oral herpes
126683671 12668367 3 Herpes simplex
126683671 12668367 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126683671 12668367 OT
126683671 12668367 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126683671 12668367 Abdominal pain upper
126683671 12668367 Arthritis
126683671 12668367 Cataract
126683671 12668367 Diarrhoea
126683671 12668367 Drug ineffective
126683671 12668367 Herpes simplex
126683671 12668367 Hip arthroplasty
126683671 12668367 Hospitalisation
126683671 12668367 Hypersensitivity
126683671 12668367 Nausea

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
126683671 12668367 1 2001 2001 0
126683671 12668367 2 2001 0