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
127064894 12706489 4 F 20160725 20160915 20160901 20160923 EXP US-PFIZER INC-2016361489 PFIZER 71.00 YR F Y 95.25000 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
127064894 12706489 1 PS VERAPAMIL HCL VERAPAMIL HYDROCHLORIDE 1 Oral 240 MG, 1X/DAY (TAKING IT AT NIGHT) 19152 240 MG MODIFIED-RELEASE TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127064894 12706489 1 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127064894 12706489 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127064894 12706489 Blood pressure inadequately controlled
127064894 12706489 Constipation
127064894 12706489 Dizziness
127064894 12706489 Dysstasia
127064894 12706489 Ear discomfort
127064894 12706489 Fall
127064894 12706489 Gait disturbance
127064894 12706489 Hair texture abnormal
127064894 12706489 Headache
127064894 12706489 Joint dislocation
127064894 12706489 Ligament rupture
127064894 12706489 Ventricular extrasystoles

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
127064894 12706489 1 20160725 0