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
125705852 12570585 2 F 2016 20160719 20160719 20160728 EXP US-ABBVIE-16K-163-1674540-00 ABBVIE 0.00 F Y 91.25000 KG 20160728 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
125705852 12570585 1 PS HUMIRA ADALIMUMAB 1 Subcutaneous 1057192 125057 40 MG SOLUTION FOR INJECTION IN PRE-FILLED PEN
125705852 12570585 2 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Oral UNKNOWN 0 20 MG QD
125705852 12570585 3 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Oral UNKNOWN 0 50 UG TABLET QD
125705852 12570585 4 C FOLIC ACID. FOLIC ACID 1 0
125705852 12570585 5 C FLONASE FLUTICASONE PROPIONATE 1 0
125705852 12570585 6 C PROBIOTIC PROBIOTICS NOS 1 0
125705852 12570585 7 C ZANTAC RANITIDINE HYDROCHLORIDE 1 0
125705852 12570585 8 C ADVAIR HFA FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 0
125705852 12570585 9 C FEXOFENADINE FEXOFENADINEFEXOFENADINE HYDROCHLORIDE 1 0
125705852 12570585 10 C ESTRADIOL. ESTRADIOL 1 0
125705852 12570585 11 C HYDROCHLOROTHIAZIDE W/TRIAMTERENE HYDROCHLOROTHIAZIDETRIAMTERENE 1 0
125705852 12570585 12 C SYSTANE (HYPROMELLOSE 2910 (4000 MPA.S)) HYPROMELLOSE 2910 (4000 MPA.S) 1 0
125705852 12570585 13 C PROAIR HFA ALBUTEROL SULFATE 1 0
125705852 12570585 14 C MAGNESIUM MAGNESIUM 1 0
125705852 12570585 15 C VITAMIN E .ALPHA.-TOCOPHEROL 1 0
125705852 12570585 16 C BIOTIN BIOTIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125705852 12570585 1 Rheumatoid arthritis
125705852 12570585 2 Rheumatoid arthritis
125705852 12570585 3 Hypothyroidism
125705852 12570585 4 Product used for unknown indication
125705852 12570585 5 Seasonal allergy
125705852 12570585 6 Gastrointestinal disorder
125705852 12570585 7 Dyspepsia
125705852 12570585 8 Allergic bronchitis
125705852 12570585 9 Seasonal allergy
125705852 12570585 10 Hormone replacement therapy
125705852 12570585 11 Fluid retention
125705852 12570585 12 Dry eye
125705852 12570585 13 Asthma
125705852 12570585 14 Muscle spasms
125705852 12570585 15 Product used for unknown indication
125705852 12570585 16 Hair disorder

Outcome of event

Event ID CASEID OUTC COD
125705852 12570585 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125705852 12570585 Alopecia
125705852 12570585 Cataract
125705852 12570585 Drug ineffective
125705852 12570585 Injection site pain
125705852 12570585 Joint swelling
125705852 12570585 Macular degeneration
125705852 12570585 Pain
125705852 12570585 Trigger finger
125705852 12570585 Visual field defect

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
125705852 12570585 1 201512 20160719 0
125705852 12570585 2 2015 0
125705852 12570585 3 2013 0