The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6661473 7307082 F 6661473-7 20100212 20100326 20100331 EXP PHEH2010US02847 NOVARTIS PHARMACEUTICAL CORPORATION 80 YR F Y 80.726 KG 20100331 MD 20100212 UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6661473 1013421405 PS TEKTURNA 1 ORAL 150 MG, QD 021985
6661473 1013421406 SS TEKTURNA 1 021985
6661473 1013421407 SS TEKTURNA 1 021985
6661473 1013421408 SS COZAAR 1 ORAL 100 MG, QD
6661473 1013421409 SS LISINOPRIL 1 ORAL 60 MG, QD
6661473 1013421410 SS LISINOPRIL 1
6661473 1013421411 SS LISINOPRIL 1
6661473 1013421412 C DIGOXIN 1 UNKNOWN UNK, UNK
6661473 1013421413 C PROTONIX 1 UNKNOWN UNK, UNK
6661473 1013421414 C LOPID 1 UNKNOWN UNK, UNK
6661473 1013421415 C CLONIDINE 1 UNKNOWN UNK, UNK
6661473 1013421416 C INSULIN 2 UNKNOWN UNK, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6661473 1013421405 HYPERTENSION
6661473 1013421406 DIABETES MELLITUS
6661473 1013421407 DIABETIC NEPHROPATHY
6661473 1013421408 HYPERTENSION
6661473 1013421409 HYPERTENSION
6661473 1013421410 DIABETES MELLITUS
6661473 1013421411 DIABETIC NEPHROPATHY

Outcome of event

Event ID OUTC COD
6661473 DE
6661473 OT

Reactions reported

Event ID PT
6661473 ANAPHYLACTIC SHOCK
6661473 ANGIOEDEMA
6661473 CARDIO-RESPIRATORY ARREST
6661473 DYSPHAGIA
6661473 DYSPNOEA
6661473 HYPOTENSION
6661473 ODYNOPHAGIA
6661473 PHARYNGEAL OEDEMA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6661473 1013421405 20080101
6661473 1013421408 20060101
6661473 1013421409 20050101