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
125875672 12587567 2 F 2007 20160112 20160725 20160726 PER US-MYLANLABS-2016M1002618 MYLAN 0.00 F Y 0.00000 20160726 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
125875672 12587567 1 PS Haloperidol Tablets, USP HALOPERIDOL 1 Oral 5 MG, UNK Y 70278 5 MG TABLET
125875672 12587567 2 SS Haloperidol Tablets, USP HALOPERIDOL 1 Oral 2 MG, QD 70278 2 MG TABLET QD
125875672 12587567 3 SS ATORVASTATIN ATORVASTATIN 1 Oral 10 MG, UNK Y 0 10 MG TABLET
125875672 12587567 4 SS BENZTROPINE MESILATE BENZTROPINE MESYLATE 1 0.5 MG, UNK 0 .5 MG
125875672 12587567 5 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Oral 500 MG, BID 0 500 MG TABLET BID

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125875672 12587567 Blood creatine phosphokinase increased
125875672 12587567 Breast enlargement
125875672 12587567 Hepatic enzyme abnormal
125875672 12587567 Hyperglycaemia
125875672 12587567 Weight increased

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
125875672 12587567 1 2007 2013 0
125875672 12587567 2 2013 0
125875672 12587567 3 201511 20151223 0
125875672 12587567 5 2012 0