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
125190281 12519028 1 I 20160620 20160701 20160701 EXP GB-ALVOGEN-2016-ALVOGEN-025548 GB-ALVOGEN-2016-ALVOGEN-025548 ALVOGEN 85.00 YR Y 0.00000 20160701 PH 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
125190281 12519028 1 PS ATENOLOL. ATENOLOL 1 Oral 18240 25 MG TABLET QD
125190281 12519028 2 SS AMLODIPINE AMLODIPINE BESYLATE 1 0 5 MG QD
125190281 12519028 3 C SIMVASTATIN. SIMVASTATIN 1 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125190281 12519028 1 Product used for unknown indication
125190281 12519028 2 Product used for unknown indication
125190281 12519028 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125190281 12519028 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125190281 12519028 Loss of consciousness
125190281 12519028 Lung infection
125190281 12519028 Nausea
125190281 12519028 Orthostatic hypotension
125190281 12519028 Syncope
125190281 12519028 Vomiting

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

no results found

Therapies reported

no results found