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
126115691 12611569 1 I 20160722 20160801 20160801 EXP CA-PURDUE PHARMA-CAN-2016-0006921 PURDUE 29.00 YR F Y 0.00000 20160727 CN CA CA

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
126115691 12611569 1 PS METHYLPHENIDATE HYDROCHLORIDE. METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK U U 205831
126115691 12611569 2 SS METHYLPHENIDATE HYDROCHLORIDE. METHYLPHENIDATE HYDROCHLORIDE 1 U U 205831
126115691 12611569 3 SS CONCERTA METHYLPHENIDATE HYDROCHLORIDE 1 Unknown UNK U U 0
126115691 12611569 4 SS XOLAIR OMALIZUMAB 1 Subcutaneous 375 MG, 1 EVERY 2 WEEKS U U 0 375 MG
126115691 12611569 5 SS XOLAIR OMALIZUMAB 1 Subcutaneous UNK U U 0
126115691 12611569 6 C AERIUS DESLORATADINE 1 Unknown UNK U U 0
126115691 12611569 7 C EPIPEN EPINEPHRINE 1 Unknown UNK U U 0
126115691 12611569 8 C PREDNISONE. PREDNISONE 1 Unknown UNK U U 0
126115691 12611569 9 C SYNTHROID LEVOTHYROXINE SODIUM 1 Unknown 50 MCG, UNK U U 0 50 UG
126115691 12611569 10 C VENTOLIN ALBUTEROL SULFATE 1 Unknown UNK U U 0
126115691 12611569 11 C VENTOLIN ALBUTEROL SULFATE 1 UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126115691 12611569 1 Impulse-control disorder
126115691 12611569 2 Disturbance in attention
126115691 12611569 3 Product used for unknown indication
126115691 12611569 4 Asthma
126115691 12611569 6 Product used for unknown indication
126115691 12611569 7 Product used for unknown indication
126115691 12611569 8 Product used for unknown indication
126115691 12611569 9 Thyroid disorder
126115691 12611569 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126115691 12611569 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126115691 12611569 Acne
126115691 12611569 Contusion
126115691 12611569 Erythema
126115691 12611569 Fatigue
126115691 12611569 Hyperthyroidism
126115691 12611569 Palpitations
126115691 12611569 Pruritus
126115691 12611569 Rash
126115691 12611569 Somnolence
126115691 12611569 Tachycardia
126115691 12611569 Weight decreased

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

no results found

Therapies reported

no results found