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
126481222 12648122 2 F 20160803 20160812 20160815 EXP PHEH2016US019698 SANDOZ 0.00 F Y 0.00000 20160815 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
126481222 12648122 1 SS DIOVAN VALSARTAN 1 Unknown 80 MG, UNK U 0 80 MG
126481222 12648122 2 PS FLUTICASONE PROPIONATE. FLUTICASONE PROPIONATE 1 Unknown UNK U 19957 SPRAY
126481222 12648122 3 SS METFORMIN METFORMIN HYDROCHLORIDE 1 Unknown UNK U 0
126481222 12648122 4 SS XOPENEX LEVALBUTEROL HYDROCHLORIDE 1 Unknown UNK U 0
126481222 12648122 5 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown 5000 U, BIW U 0 5000 DF CAPSULE QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126481222 12648122 1 Product used for unknown indication
126481222 12648122 2 Product used for unknown indication
126481222 12648122 3 Product used for unknown indication
126481222 12648122 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126481222 12648122 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126481222 12648122 Asthma
126481222 12648122 Drug intolerance
126481222 12648122 Dyspnoea
126481222 12648122 Nasal congestion
126481222 12648122 Pruritus
126481222 12648122 Somnolence
126481222 12648122 Weight decreased
126481222 12648122 Weight increased

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

no results found

Therapies reported

no results found