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
119638984 11963898 4 F 2012 20160712 20160126 20160721 EXP US-ABBVIE-15K-163-1378859-00 ABBVIE 63.63 YR F Y 59.02000 KG 20160721 CN COUNTRY NOT SPECIFIED 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
119638984 11963898 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous Y U UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
119638984 11963898 2 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y U UNKNOWN 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE QOW
119638984 11963898 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous Y U UNKNOWN 125057 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
119638984 11963898 4 SS WELLBUTRIN BUPROPION HYDROCHLORIDE 1 Unknown UNKNOWN 0
119638984 11963898 5 C PEPCID FAMOTIDINE 1 0
119638984 11963898 6 C KLONOPIN CLONAZEPAM 1 Oral 0
119638984 11963898 7 C METOCLOPRAMIDE. METOCLOPRAMIDE 1 0
119638984 11963898 8 C XANAX ALPRAZOLAM 1 0
119638984 11963898 9 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 0
119638984 11963898 10 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 0
119638984 11963898 11 C VITAMINS NOS VITAMINS 1 0
119638984 11963898 12 C TYLENOL EXTRA STRENGTH ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119638984 11963898 1 Psoriatic arthropathy
119638984 11963898 2 Psoriasis
119638984 11963898 3 Psoriasis
119638984 11963898 4 Depression
119638984 11963898 5 Gastritis
119638984 11963898 6 Anxiety
119638984 11963898 7 Gastritis
119638984 11963898 8 Insomnia
119638984 11963898 9 Insomnia
119638984 11963898 10 Depression
119638984 11963898 11 Product used for unknown indication
119638984 11963898 12 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119638984 11963898 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119638984 11963898 Anxiety
119638984 11963898 Arthralgia
119638984 11963898 Burning sensation
119638984 11963898 Chest discomfort
119638984 11963898 Dizziness
119638984 11963898 Drug ineffective
119638984 11963898 Dry mouth
119638984 11963898 Dysuria
119638984 11963898 Ear discomfort
119638984 11963898 Fatigue
119638984 11963898 Feeling hot
119638984 11963898 Fibromyalgia
119638984 11963898 Gingival pain
119638984 11963898 Hypersensitivity
119638984 11963898 Hypoaesthesia
119638984 11963898 Injection site erythema
119638984 11963898 Intervertebral disc protrusion
119638984 11963898 Muscle tightness
119638984 11963898 Mycotic allergy
119638984 11963898 Nasal discomfort
119638984 11963898 Nerve injury
119638984 11963898 Neuralgia
119638984 11963898 Oral discomfort
119638984 11963898 Pain in jaw
119638984 11963898 Paraesthesia
119638984 11963898 Paraesthesia oral
119638984 11963898 Psoriasis
119638984 11963898 Psoriatic arthropathy
119638984 11963898 Seasonal allergy
119638984 11963898 Small fibre neuropathy
119638984 11963898 Thirst

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
119638984 11963898 1 2006 0
119638984 11963898 2 2008 20150426 0
119638984 11963898 3 20150802 0