The Safety Rates Drug Report

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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
127000491 12700049 1 I 20160422 20160830 20160830 EXP GB-PRESTIUM-2016RN000364 RENAISSANCE 0.00 Y 0.00000 20160830 MD 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
127000491 12700049 1 PS Aciclovir ACYCLOVIR 1 Unknown 400 MG, UNK U 20089 400 MG TABLET
127000491 12700049 2 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 400 MG, UNK U 0 400 MG TABLET
127000491 12700049 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 150 MG, UNK U 0 150 MG TABLET
127000491 12700049 4 SS MARAVIROC MARAVIROC 1 Unknown 300 MG, UNK U 0 300 MG
127000491 12700049 5 SS VIRAMUNE NEVIRAPINE 1 Unknown 400 MG, UNK, PR U 0 400 MG
127000491 12700049 6 C ALPROSTADIL. ALPROSTADIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127000491 12700049 1 Product used for unknown indication
127000491 12700049 2 Product used for unknown indication
127000491 12700049 4 Product used for unknown indication
127000491 12700049 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127000491 12700049 HO
127000491 12700049 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127000491 12700049 Dizziness
127000491 12700049 Meniere's disease

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found