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
122413303 12241330 3 F 20160308 20160512 20160406 20160819 PER US-ASTRAZENECA-2016SE27913 ASTRAZENECA 29983.00 DY F Y 49.90000 KG 20160819 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
122413303 12241330 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80/4.5 MCG, TWO TIMES A DAY 2000347C00 21929
122413303 12241330 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 80/4.5 MCG, TWO TIMES A DAY 2000347C00 21929
122413303 12241330 3 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Respiratory (inhalation) DAILY 0
122413303 12241330 4 C FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 DAILY 0
122413303 12241330 5 C NASAL WASH 2 DAILY 0
122413303 12241330 6 C BLOOD THINNER UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122413303 12241330 1 Emphysema
122413303 12241330 2 Emphysema
122413303 12241330 3 Emphysema
122413303 12241330 4 Sinus disorder
122413303 12241330 5 Sinus disorder
122413303 12241330 6 Anticoagulant therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122413303 12241330 Cough
122413303 12241330 Drug dose omission
122413303 12241330 Fatigue
122413303 12241330 Influenza
122413303 12241330 Pain
122413303 12241330 Product quality issue

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
122413303 12241330 1 2006 0
122413303 12241330 2 201602 0