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
126698271 12669827 1 I 201608 20160815 20160819 20160819 EXP GB-MHRA-TPP13985770C1775729YC1470406759488 GB-PFIZER INC-2016388270 PFIZER 30.00 YR F Y 77.00000 KG 20160819 MD GB GB

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
126698271 12669827 1 PS SERTRALINE HCL SERTRALINE HYDROCHLORIDE 1 UNK U 19839
126698271 12669827 2 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 1 DF, 1X/DAY 1 DF 0 1 DF QD
126698271 12669827 3 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 USE AS DIRECTED 0
126698271 12669827 4 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 2 DF, 4X/DAY 80 DF 0 2 DF QID

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126698271 12669827 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126698271 12669827 Asthma
126698271 12669827 Bronchospasm
126698271 12669827 Condition aggravated

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
126698271 12669827 1 20160805 0
126698271 12669827 2 20160805 0
126698271 12669827 3 20160726 0
126698271 12669827 4 20160726 20160727 0