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
126764801 12676480 1 I 2016 20160809 20160823 20160823 PER US-GLAXOSMITHKLINE-US2016GSK115859 GLAXOSMITHKLINE 0.00 F Y 0.00000 20160823 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
126764801 12676480 1 PS LAMICTAL LAMOTRIGINE 1 UNK UNK, U UNKNOWN 20241
126764801 12676480 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous 2 IN 1 ONCE UNKNOWN 0 SOLUTION FOR INJECTION
126764801 12676480 3 SS TRINTELLIX VORTIOXETINE HYDROBROMIDE 1 UNK UNK, U UNKNOWN 0
126764801 12676480 4 SS LEXAPRO ESCITALOPRAM OXALATE 1 UNK UNK, U UNKNOWN 0
126764801 12676480 5 SS ZYPREXA OLANZAPINE 1 UNK UNK, U UNKNOWN 0
126764801 12676480 6 C ATIVAN LORAZEPAM 1 UNK UNK, U U UNKNOWN 0
126764801 12676480 7 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK UNK, U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126764801 12676480 1 Bipolar disorder
126764801 12676480 2 Psoriasis
126764801 12676480 3 Depression
126764801 12676480 4 Product used for unknown indication
126764801 12676480 5 Bipolar disorder
126764801 12676480 6 Anxiety
126764801 12676480 7 Gastrooesophageal reflux disease

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126764801 12676480 Drug interaction
126764801 12676480 Nausea
126764801 12676480 Respiratory tract congestion
126764801 12676480 Throat irritation
126764801 12676480 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
126764801 12676480 2 201602 0