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
127741891 12774189 1 I 2016 20160914 20160923 20160923 PER US-PFIZER INC-2016434485 PFIZER 81.00 YR F Y 72.56000 KG 20160923 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
127741891 12774189 1 PS VERAPAMIL HCL VERAPAMIL HYDROCHLORIDE 1 Oral 0.5 DF, 4X/DAY (40 MG, 90 COUNT) 18817 .5 DF FILM-COATED TABLET QID

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127741891 12774189 Activities of daily living impaired
127741891 12774189 Asthenia
127741891 12774189 Dizziness
127741891 12774189 Drug effect decreased
127741891 12774189 Drug ineffective
127741891 12774189 Drug intolerance
127741891 12774189 Heart rate decreased
127741891 12774189 Heart rate irregular
127741891 12774189 Intentional product misuse
127741891 12774189 Neuralgia
127741891 12774189 Poor quality drug administered
127741891 12774189 Product physical issue
127741891 12774189 Product use issue
127741891 12774189 Wrong technique in product usage process

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

no results found

Therapies reported

no results found