The Safety Rates Drug Report

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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
126904351 12690435 1 I 20160822 20160826 20160826 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-069937 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160826 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
126904351 12690435 1 PS ABILIFY ARIPIPRAZOLE 1 Oral UNK, QD N 21436 QD
126904351 12690435 2 SS PAXIL PAROXETINE HYDROCHLORIDE 1 N 0
126904351 12690435 3 SS PAXIL PAROXETINE HYDROCHLORIDE 1 N 0
126904351 12690435 4 SS PAROXETINE. PAROXETINE 1 Unknown UNK N 0
126904351 12690435 5 SS PAROXETINE. PAROXETINE 1 N 0
126904351 12690435 6 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 1 DF, UNK U 0 1 DF
126904351 12690435 7 C TRIAMTERENE AND HYDROCHLOROTHIAZID HYDROCHLOROTHIAZIDETRIAMTERENE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126904351 12690435 1 Major depression
126904351 12690435 2 Depression
126904351 12690435 3 Anxiety
126904351 12690435 4 Depression
126904351 12690435 5 Anxiety
126904351 12690435 6 Product used for unknown indication
126904351 12690435 7 Hypertension

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126904351 12690435 Depression
126904351 12690435 Drug ineffective
126904351 12690435 Malaise

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

no results found

Therapies reported

no results found