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
124302222 12430222 2 F 201602 20160624 20160602 20160701 EXP US-ASTRAZENECA-2016SE56471 ASTRAZENECA 820.00 MON F Y 72.60000 KG 20160701 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
124302222 12430222 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG TWICE DAILY 21929 BID
124302222 12430222 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG TWICE DAILY 3001097C00 21929 BID
124302222 12430222 3 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 UG TWICE DAILY 3001097C00 21929 BID
124302222 12430222 4 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) 230 21, 2 PUFFS TWICE A DAY 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124302222 12430222 1 Asthma
124302222 12430222 2 Asthma
124302222 12430222 3 Asthma
124302222 12430222 4 Asthma

Outcome of event

Event ID CASEID OUTC COD
124302222 12430222 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124302222 12430222 Asthma
124302222 12430222 Device malfunction
124302222 12430222 Drug dose omission
124302222 12430222 Malaise
124302222 12430222 White blood cell count increased

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
124302222 12430222 1 201601 0
124302222 12430222 2 201602 0
124302222 12430222 3 201603 0
124302222 12430222 4 20160517 0