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
123875622 12387562 2 F 20160628 20160520 20160701 PER PHEH2016US012294 NOVARTIS 0.00 F Y 0.00000 20160701 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
123875622 12387562 1 PS DIOVAN VALSARTAN 1 Oral 160 MG, QD U 20665 160 MG QD
123875622 12387562 2 C ATENOLOL. ATENOLOL 1 Unknown 25 MG, QD (HALF OF A 25MG PILL) U 0 25 MG QD
123875622 12387562 3 C IMIPRAMINE IMIPRAMINE 1 Oral 25 MG, QD (25MG, HALF OF IT) U 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123875622 12387562 1 Product used for unknown indication
123875622 12387562 2 Product used for unknown indication
123875622 12387562 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123875622 12387562 Drug hypersensitivity
123875622 12387562 Erythema
123875622 12387562 Headache
123875622 12387562 Nausea
123875622 12387562 Product colour issue
123875622 12387562 Pruritus
123875622 12387562 Skin sensitisation

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

no results found

Therapies reported

no results found