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
124407732 12440773 2 F 20160220 20160630 20160606 20160707 EXP CH-SM-2016-04233 CH-UCBSA-2016020347 UCB 87.18 YR M Y 0.00000 20160707 MD CH CH

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
124407732 12440773 1 PS KEPPRA LEVETIRACETAM 1 Oral 500 MG TWICE A DAY Y 21035 500 MG BID
124407732 12440773 2 SS KEPPRA LEVETIRACETAM 1 750 MG, 2X/DAY (BID), DOSE INCREASED Y 21035 750 MG BID
124407732 12440773 3 SS KEPPRA LEVETIRACETAM 1 500 MG, 2X/DAY (BID),DOSE DECREASED Y 21035 500 MG BID
124407732 12440773 4 SS KEPPRA LEVETIRACETAM 1 250 MG, 2X/DAY (BID) Y 21035 250 MG BID
124407732 12440773 5 SS Liquemin HEPARIN SODIUM 1 Intravenous drip UNK Y U 0
124407732 12440773 6 SS SIMVASTATIN. SIMVASTATIN 1 Oral 40 MG DAILY DOSE Y U 0
124407732 12440773 7 SS Sifrol PRAMIPEXOLE 1 Oral 0.13 MG ONCE DAILY Y U 0 .13 MG QD
124407732 12440773 8 SS Sifrol PRAMIPEXOLE 1 0.26 MG, ONCE DAILY (QD) Y U 0 .26 MG QD
124407732 12440773 9 SS Sifrol PRAMIPEXOLE 1 GRADUAL REDUCTION Y U 0
124407732 12440773 10 SS SINTROM ACENOCOUMAROL 1 Oral UNK U 0
124407732 12440773 11 SS Clexane ENOXAPARIN SODIUM 1 Subcutaneous 40 MG ONCE DAILY Y U 0 40 MG QD
124407732 12440773 12 SS Clexane ENOXAPARIN SODIUM 1 60 MG, 2X/DAY (BID) Y U 0 60 MG BID
124407732 12440773 13 SS Aspirin cardio ASPIRIN 1 Oral 100 MG ONCE DAILY Y U 0 100 MG QD
124407732 12440773 14 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 40 MG ONCE DAILY Y U 0 40 MG QD
124407732 12440773 15 C Pradif TAMSULOSIN HYDROCHLORIDE 1 Oral 400 MG ONCE DAILY U U 0 400 UG QD
124407732 12440773 16 C LAMICTAL LAMOTRIGINE 1 Oral 25 MG, ONCE DAILY (QD) Y U 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124407732 12440773 1 Epilepsy
124407732 12440773 5 Anticoagulant therapy
124407732 12440773 6 Cerebrovascular accident
124407732 12440773 7 Restless legs syndrome
124407732 12440773 10 Anticoagulant therapy
124407732 12440773 11 Product used for unknown indication
124407732 12440773 13 Product used for unknown indication
124407732 12440773 14 Product used for unknown indication
124407732 12440773 15 Product used for unknown indication
124407732 12440773 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124407732 12440773 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124407732 12440773 Muscle haemorrhage
124407732 12440773 Thrombocytopenia

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
124407732 12440773 1 20160209 201602 0
124407732 12440773 2 20160211 2016 0
124407732 12440773 3 20160302 201603 0
124407732 12440773 4 20160307 201603 0
124407732 12440773 5 20160222 20160307 0
124407732 12440773 6 20160207 20160401 0
124407732 12440773 7 20160118 2016 0
124407732 12440773 8 20160304 201603 0
124407732 12440773 9 201603 20160308 0
124407732 12440773 10 20160303 20160415 0
124407732 12440773 11 20160102 201602 0
124407732 12440773 12 20160219 0
124407732 12440773 13 20160219 0
124407732 12440773 14 20160208 20160223 0
124407732 12440773 15 20160103 0
124407732 12440773 16 20160307 201603 0