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
124846673 12484667 3 F 20160513 20160617 20160621 20160714 EXP US-FRI-1000085498 FOREST 51.89 YR M Y 0.00000 20160714 MD 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
124846673 12484667 1 PS LEXAPRO ESCITALOPRAM OXALATE 1 Oral 20 MG, QD 5940 MG 21323 20 MG TABLET QD
124846673 12484667 2 SS BLINDED INVESTIGATIONAL MEDICINAL PRODUCT (IMP) NON-PARTNER INVESTIGATIONAL PRODUCT 1 Oral UNK 0 TABLET
124846673 12484667 3 C LISINOPRIL. LISINOPRIL 1 Oral 40 MG, QD 0 40 MG QD
124846673 12484667 4 C ALBUTEROL. ALBUTEROL 1 Respiratory (inhalation) 2 PUFFS , PRN 0
124846673 12484667 5 C ATENOLOL. ATENOLOL 1 Oral 25 MG, QD 0 25 MG QD
124846673 12484667 6 C SIMVASTATIN. SIMVASTATIN 1 Oral 20 MG, QD 0 20 MG QD
124846673 12484667 7 C LORATADINE. LORATADINE 1 Oral 10 MG, QD 0 10 MG QD
124846673 12484667 8 C FLONASE FLUTICASONE PROPIONATE 1 Nasal 50 ?G, QD (2 SPRAYS) 0 50 UG QD
124846673 12484667 9 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Oral 0.4 MG, QD 0 .4 MG QD
124846673 12484667 10 C RANITIDINE. RANITIDINE 1 Oral 300 MG, QD 0 300 MG QD
124846673 12484667 11 C FLOVENT FLUTICASONE PROPIONATE 1 Respiratory (inhalation) 2 PUFFS, BID 0 BID
124846673 12484667 12 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, QD 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124846673 12484667 1 Major depression
124846673 12484667 2 Major depression
124846673 12484667 3 Hypertension
124846673 12484667 4 Asthma
124846673 12484667 5 Hypertension
124846673 12484667 6 Blood cholesterol increased
124846673 12484667 7 Hypersensitivity
124846673 12484667 8 Hypersensitivity
124846673 12484667 9 Prostatomegaly
124846673 12484667 10 Gastrooesophageal reflux disease
124846673 12484667 11 Asthma
124846673 12484667 12 Gastrooesophageal reflux disease

Outcome of event

Event ID CASEID OUTC COD
124846673 12484667 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124846673 12484667 Abdominal pain
124846673 12484667 Dizziness
124846673 12484667 Mitral valve incompetence

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
124846673 12484667 1 20150722 20160517 0
124846673 12484667 2 20151118 20160517 0
124846673 12484667 3 2008 0
124846673 12484667 4 1988 0
124846673 12484667 5 2013 0
124846673 12484667 6 2010 0
124846673 12484667 7 2010 0
124846673 12484667 8 201406 0
124846673 12484667 9 20150728 0
124846673 12484667 10 20151027 0
124846673 12484667 11 20151101 0
124846673 12484667 12 20160128 0