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
76277112 7627711 2 F 2010 20160909 20101013 20160923 PER US-ASTRAZENECA-2010SE19725 ASTRAZENECA 71.00 YR F Y 90.70000 KG 20160923 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
76277112 7627711 1 PS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 2 PUFFS U 21929 BID
76277112 7627711 2 SS SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Respiratory (inhalation) 160/4.5 1 PUFF U 21929
76277112 7627711 3 SS MOVANTIK NALOXEGOL OXALATE 1 Oral 0 25 MG TABLET QD
76277112 7627711 4 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
76277112 7627711 5 C MORPHINE MORPHINE 1 0
76277112 7627711 6 C OXYCODONE OXYCODONE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
76277112 7627711 1 Pleural effusion
76277112 7627711 2 Pleural effusion
76277112 7627711 3 Constipation
76277112 7627711 4 Thyroid disorder
76277112 7627711 5 Back disorder
76277112 7627711 6 Back disorder

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
76277112 7627711 Drug dose omission
76277112 7627711 Drug ineffective
76277112 7627711 Intraocular pressure increased
76277112 7627711 Rectal haemorrhage

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
76277112 7627711 1 2010 0
76277112 7627711 3 201606 0