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
126819001 12681900 1 I 20160504 20160824 20160824 EXP GB-MYLANLABS-2016M1018801 MYLAN 0.00 Y 0.00000 20160824 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
126819001 12681900 1 PS ACICLOVIR ACYCLOVIR 1 Unknown 400 MG, UNK U U 75211 400 MG TABLET
126819001 12681900 2 SS LAMIVUDINE. LAMIVUDINE 1 Unknown 150 MG, UNK U U 0 150 MG TABLET
126819001 12681900 3 SS MARAVIROC MARAVIROC 1 Unknown 300 MG, UNK U U 0 300 MG TABLET
126819001 12681900 4 SS VIRAMUNE NEVIRAPINE 1 Unknown 400 MG, UNK U U 0 400 MG TABLET
126819001 12681900 5 C ALPROSTADIL. ALPROSTADIL 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126819001 12681900 1 Product used for unknown indication
126819001 12681900 2 Product used for unknown indication
126819001 12681900 3 Product used for unknown indication
126819001 12681900 4 Product used for unknown indication
126819001 12681900 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126819001 12681900 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126819001 12681900 Dizziness
126819001 12681900 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