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
126565081 12656508 1 I 2016 20160808 20160816 20160816 PER US-TAKEDA-2016TUS013973 TAKEDA 0.00 F Y 0.00000 20160816 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
126565081 12656508 1 PS TRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown UNK 204447 TABLET
126565081 12656508 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous UNK UNK, QD 0 SOLUTION FOR INJECTION QD
126565081 12656508 3 SS LEXAPRO ESCITALOPRAM OXALATE 1 Unknown UNK 0
126565081 12656508 4 SS LAMICTAL LAMOTRIGINE 1 Unknown UNK 0
126565081 12656508 5 SS ZYPREXA OLANZAPINE 1 Unknown UNK 0
126565081 12656508 6 C ATIVAN LORAZEPAM 1 UNK U 0
126565081 12656508 7 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126565081 12656508 1 Depression
126565081 12656508 2 Psoriasis
126565081 12656508 3 Product used for unknown indication
126565081 12656508 4 Bipolar disorder
126565081 12656508 5 Bipolar disorder
126565081 12656508 6 Anxiety
126565081 12656508 7 Reflux gastritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126565081 12656508 Nausea
126565081 12656508 Respiratory tract congestion
126565081 12656508 Throat irritation
126565081 12656508 Vomiting

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
126565081 12656508 2 201602 0