The Safety Rates Drug Report

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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
125418601 12541860 1 I 201603 20160627 20160708 20160708 PER US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-41659BP BOEHRINGER INGELHEIM 71.91 YR F Y 0.00000 20160708 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
125418601 12541860 1 PS MICARDIS TELMISARTAN 1 Oral 160 MG 20850 80 MG TABLET BID
125418601 12541860 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 150 MCG 0 150 UG TABLET QD
125418601 12541860 3 C VERAPAMIL VERAPAMIL HYDROCHLORIDE 1 Oral 300 MG 0 300 MG TABLET QD
125418601 12541860 4 C Atorvastatin ATORVASTATIN 1 Oral 20 MG 0 20 MG TABLET QD
125418601 12541860 5 C VITAMIN B12 CYANOCOBALAMIN 1 Oral 1 ANZ 0 TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125418601 12541860 1 Hypertension
125418601 12541860 2 Hypothyroidism
125418601 12541860 3 Product used for unknown indication
125418601 12541860 4 Blood cholesterol increased
125418601 12541860 5 Supplementation therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125418601 12541860 Lip swelling
125418601 12541860 Productive cough
125418601 12541860 Swelling face
125418601 12541860 Swollen tongue

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
125418601 12541860 1 1996 0
125418601 12541860 4 2006 0
125418601 12541860 5 201604 0