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
126205821 12620582 1 I 20160514 20160720 20160804 20160804 EXP IT-APOTEX-2016AP010089 APOTEX 75.00 YR F Y 0.00000 20160804 CN IT IT

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
126205821 12620582 1 PS PAXIL PAROXETINE HYDROCHLORIDE 1 Oral 1 DF, QD U U 20031 1 DF TABLET QD
126205821 12620582 2 SS TRIATEC /00885601/ RAMIPRIL 1 Oral 1 DF, QD U U 0 1 DF QD
126205821 12620582 3 SS AMIODARONE AMIODARONE 1 Oral 1 DF, QD U U 0 1 DF QD
126205821 12620582 4 SS PEPTAZOL /01263204/ PANTOPRAZOLE SODIUM 1 Oral 1 DF, QD U U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126205821 12620582 1 Depression
126205821 12620582 2 Hypertension
126205821 12620582 3 Tachycardia
126205821 12620582 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126205821 12620582 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126205821 12620582 Dyspnoea
126205821 12620582 Hypertensive crisis

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

no results found

Therapies reported

no results found