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
123908353 12390835 3 F 20160310 20160823 20160520 20160830 EXP FR-AFSSAPS-NY20160810 FR-GLAXOSMITHKLINE-FR2016GSK071162 GLAXOSMITHKLINE 69.00 YR M Y 0.00000 20160830 OT FR FR

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
123908353 12390835 1 PS Zelitrex VALACYCLOVIR HYDROCHLORIDE 1 Oral 500 MG, 1D 20487 500 MG QD
123908353 12390835 2 SS BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral UNK Y 0 TABLET
123908353 12390835 3 SS ZYDELIG IDELALISIB 1 Oral 150 MG, BID 8400 MG Y 0 150 MG BID
123908353 12390835 4 SS CALCIPARINE HEPARIN CALCIUM 1 UNK Y 0
123908353 12390835 5 SS lasilix retard FUROSEMIDE 1 UNK U 0 CAPSULE
123908353 12390835 6 SS LOXEN NICARDIPINE HYDROCHLORIDE 1 Oral 50 MG, BID Y U 0 50 MG BID
123908353 12390835 7 SS CORDARONE AMIODARONE HYDROCHLORIDE 1 Oral 200 MG, UNK 0 200 MG TABLET
123908353 12390835 8 SS Lasilix FUROSEMIDE 1 Oral UNK Y U 0
123908353 12390835 9 SS TAHOR ATORVASTATIN CALCIUM 1 Oral UNK Y U 0
123908353 12390835 10 SS Amlor AMLODIPINE BESYLATE 1 Oral 5 MG, 1D 60 MG Y U 0 5 MG CAPSULE QD
123908353 12390835 11 C DEXAMETHASONE. DEXAMETHASONE 1 0
123908353 12390835 12 C Triatec RAMIPRIL 1 1.25 MG, UNK 0 1.25 MG TABLET
123908353 12390835 13 C Ventoline ALBUTEROL 1 UNK U 0
123908353 12390835 14 C ATROVENT IPRATROPIUM BROMIDE 1 UNK U 0
123908353 12390835 15 C EUPANTOL PANTOPRAZOLE SODIUM 1 UNK U 0
123908353 12390835 16 C DEXAMETHASONE. DEXAMETHASONE 1 UNK U 0
123908353 12390835 17 C DUPHALAC LACTULOSE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123908353 12390835 1 Product used for unknown indication
123908353 12390835 2 Product used for unknown indication
123908353 12390835 3 Product used for unknown indication
123908353 12390835 4 Product used for unknown indication
123908353 12390835 5 Product used for unknown indication
123908353 12390835 6 Hypertension
123908353 12390835 7 Product used for unknown indication
123908353 12390835 8 Product used for unknown indication
123908353 12390835 9 Product used for unknown indication
123908353 12390835 10 Hypertension
123908353 12390835 13 Product used for unknown indication
123908353 12390835 14 Product used for unknown indication
123908353 12390835 15 Product used for unknown indication
123908353 12390835 16 Product used for unknown indication
123908353 12390835 17 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123908353 12390835 OT
123908353 12390835 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123908353 12390835 Dermatitis exfoliative

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
123908353 12390835 1 20160211 0
123908353 12390835 2 20160211 20160318 0
123908353 12390835 3 20160211 20160603 0
123908353 12390835 4 20160229 20160411 0
123908353 12390835 5 20160411 0
123908353 12390835 6 20160422 20160603 0
123908353 12390835 7 20160524 0
123908353 12390835 8 20160211 20160531 0
123908353 12390835 9 20160201 20160422 0
123908353 12390835 10 20160227 20160411 0