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
125655062 12565506 2 F 20160816 20160718 20160819 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-46362BP BOEHRINGER INGELHEIM 0.00 M Y 0.00000 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
125655062 12565506 1 PS ATROVENT IPRATROPIUM BROMIDE 1 Respiratory (inhalation) U 1501888 OR 0,NO597008717 21527 INHALATION SOLUTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125655062 12565506 1 Chronic obstructive pulmonary disease

Outcome of event

Event ID CASEID OUTC COD
125655062 12565506 LT
125655062 12565506 HO
125655062 12565506 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125655062 12565506 Acute kidney injury
125655062 12565506 Acute respiratory distress syndrome
125655062 12565506 Acute respiratory failure
125655062 12565506 Asthma
125655062 12565506 Bronchitis
125655062 12565506 Chronic obstructive pulmonary disease
125655062 12565506 Gastrointestinal disorder
125655062 12565506 Hyperglycaemia
125655062 12565506 Hypertension
125655062 12565506 Hypokalaemia
125655062 12565506 Lung disorder
125655062 12565506 Respiratory distress
125655062 12565506 Sinusitis
125655062 12565506 Status asthmaticus
125655062 12565506 Urinary tract infection

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

no results found

Therapies reported

no results found