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
91689043 9168904 3 F 20160711 20130318 20160728 EXP US-ASTRAZENECA-2013SE16420 ASTRAZENECA 81.00 YR F Y 0.00000 20160728 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
91689043 9168904 1 PS ATACAND CANDESARTAN CILEXETIL 1 Oral U 0 TABLET
91689043 9168904 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) U 0
91689043 9168904 3 SS ZESTRIL LISINOPRIL 1 Oral U 0 TABLET
91689043 9168904 4 SS TOPROL XL METOPROLOL SUCCINATE 1 Oral U 0 MODIFIED-RELEASE TABLET
91689043 9168904 5 C ADVAIR DISKUS FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown U 0
91689043 9168904 6 C LOVAZA OMEGA-3-ACID ETHYL ESTERS 1 Oral 0 2 DF CAPSULE BID
91689043 9168904 7 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0 1 DF TABLET QD
91689043 9168904 8 C METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 1 TABLET IN THE MORNING AND 2 AT NIGHT 0 TABLET
91689043 9168904 9 C ASPIRIN. ASPIRIN 1 0 1 DF CHEWABLE TABLET QD
91689043 9168904 10 C GABAPENTIN. GABAPENTIN 1 1.0DF UNKNOWN 0 1 DF CAPSULE
91689043 9168904 11 C TRAZODONE HYDROCHLORIDE. TRAZODONE HYDROCHLORIDE 1 0 .5 DF TABLET QD
91689043 9168904 12 C CRESTOR ROSUVASTATIN CALCIUM 1 Oral 0 1 DF TABLET QOD
91689043 9168904 13 C ZANTAC RANITIDINE HYDROCHLORIDE 1 Oral 0 1 DF TABLET BID
91689043 9168904 14 C TYLENOL ARTHRITIS PAIN ACETAMINOPHEN 1 0 2 DF BID
91689043 9168904 15 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 0 1 DF TABLET QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
91689043 9168904 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
91689043 9168904 Adverse event
91689043 9168904 Angioedema
91689043 9168904 Drug hypersensitivity
91689043 9168904 Dyspnoea
91689043 9168904 Rash

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

no results found

Therapies reported

no results found