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
125485742 12548574 2 F 201605 20160628 20160712 20160822 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-42148BP BOEHRINGER INGELHEIM 66.32 YR M Y 0.00000 20160822 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
125485742 12548574 1 PS MICARDIS TELMISARTAN 1 Oral 20 MG Y 558016 20850 20 MG TABLET QD
125485742 12548574 2 SS MICARDIS TELMISARTAN 1 Oral STRENGTH: 20 MG; HALF PILL Y 558016 20850 TABLET QD
125485742 12548574 3 C HYDROCHORATHIZIDE 2 Oral 25 MG 0 25 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125485742 12548574 1 Hypertension
125485742 12548574 3 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125485742 12548574 Arthralgia
125485742 12548574 Blood pressure decreased
125485742 12548574 Contusion
125485742 12548574 Headache
125485742 12548574 Incorrect dose administered
125485742 12548574 Joint stiffness

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
125485742 12548574 1 20160312 201606 0