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
125806913 12580691 3 F 20160801 20160721 20160815 EXP GB-WATSON-2016-15593 ACTAVIS 61.00 YR M Y 0.00000 20160815 OT GB GB

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
125806913 12580691 1 SS Amitriptyline AMITRIPTYLINE 1 Oral UNK U UNCONFIRMED 0
125806913 12580691 2 SS Mirtazapine (Unknown) MIRTAZAPINE 1 Oral UNK U UNCONFIRMED 0 UNK
125806913 12580691 3 PS Gabapentin (Unknown) GABAPENTIN 1 Unknown UNK U UNCONFIRMED 75350 UNK
125806913 12580691 4 SS SIMPONI GOLIMUMAB 1 Subcutaneous 50 MG, ONCE A MONTH 0 50 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125806913 12580691 1 Product used for unknown indication
125806913 12580691 2 Product used for unknown indication
125806913 12580691 3 Product used for unknown indication
125806913 12580691 4 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
125806913 12580691 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125806913 12580691 Anxiety
125806913 12580691 Arrhythmia
125806913 12580691 Depression
125806913 12580691 Dysphonia
125806913 12580691 Erectile dysfunction
125806913 12580691 Headache
125806913 12580691 Musculoskeletal stiffness
125806913 12580691 Psoriatic arthropathy

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

no results found

Therapies reported

no results found