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
96954417 9695441 7 F 201310 20160825 20131119 20160830 EXP PHHY2013FR131701 NOVARTIS 55.00 YR M Y 0.00000 20160830 MD 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
96954417 9695441 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD (28 TABLETS) 22334 10 MG QD
96954417 9695441 2 C MEDROL METHYLPREDNISOLONE 1 Oral 3 DF, QD 0 3 DF TABLET QD
96954417 9695441 3 C OXYNORM OXYCODONE HYDROCHLORIDE 1 Oral 10 MG, BID 0 10 MG BID
96954417 9695441 4 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Oral 90 MG, BID 0 90 MG BID
96954417 9695441 5 C MACROGOL POLYETHYLENE GLYCOLS 1 Oral 5.9 G, QID 0 5.9 G QID
96954417 9695441 6 C LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous 0.4 ML, QD 0 .4 ML INJECTION QD
96954417 9695441 7 C DIFFU-K POTASSIUM CHLORIDE 1 Oral 600 MG, BID 0 600 MG BID
96954417 9695441 8 C FENOFIBRATE. FENOFIBRATE 1 Oral 500 MG, QD 0 500 MG QD
96954417 9695441 9 C DOLIPRANE ACETAMINOPHEN 1 Oral 1 G, QID 0 1 G QID
96954417 9695441 10 C NEBIVOLOL. NEBIVOLOL 1 Oral 5 MG, QD 0 5 MG QD
96954417 9695441 11 C ALPRESS PRAZOSIN 1 Oral 5 MG, QD 0 5 MG QD
96954417 9695441 12 C LYRICA PREGABALIN 1 Oral 75 MG, BID 0 75 MG BID
96954417 9695441 13 C GAVISCON ALUMINUM HYDROXIDEMAGNESIUM CARBONATE 1 Oral 3 DF, QD 0 3 DF QD
96954417 9695441 14 C INEXIUM//ESOMEPRAZOLE SODIUM ESOMEPRAZOLE SODIUM 1 Oral 40 MG, QD 0 40 MG QD
96954417 9695441 15 C BROMAZEPAM BROMAZEPAM 1 Oral 6 MG, TID 0 6 MG TABLET TID
96954417 9695441 16 C PRIMPERAN METOCLOPRAMIDE HYDROCHLORIDE 1 Oral 10 MG, TID 0 10 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
96954417 9695441 1 Renal cancer
96954417 9695441 2 Antiinflammatory therapy
96954417 9695441 3 Pain
96954417 9695441 4 Pain
96954417 9695441 5 Constipation
96954417 9695441 6 Coagulopathy
96954417 9695441 7 Hypokalaemia
96954417 9695441 8 Hypertriglyceridaemia
96954417 9695441 9 Pain
96954417 9695441 10 Hypertension
96954417 9695441 11 Hypertension
96954417 9695441 12 Pain
96954417 9695441 13 Gastrooesophageal reflux disease
96954417 9695441 14 Gastrooesophageal reflux disease
96954417 9695441 15 Anxiety
96954417 9695441 16 Antiemetic supportive care

Outcome of event

Event ID CASEID OUTC COD
96954417 9695441 OT
96954417 9695441 DE
96954417 9695441 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
96954417 9695441 Confusional state
96954417 9695441 General physical health deterioration
96954417 9695441 Hypoxia
96954417 9695441 Lung disorder
96954417 9695441 Musculoskeletal chest pain
96954417 9695441 Nervous system disorder
96954417 9695441 Pyrexia
96954417 9695441 Respiratory disorder
96954417 9695441 Septic shock
96954417 9695441 Spinal cord compression
96954417 9695441 Urinary retention

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
96954417 9695441 1 20131002 201310 0
96954417 9695441 2 201307 0
96954417 9695441 3 20130506 0
96954417 9695441 4 20130410 0
96954417 9695441 5 20130410 0
96954417 9695441 6 20130410 0
96954417 9695441 7 20130410 0
96954417 9695441 8 20130410 0
96954417 9695441 9 20130327 0
96954417 9695441 10 20130327 0
96954417 9695441 11 20121115 0
96954417 9695441 12 20130327 0
96954417 9695441 13 20130327 0
96954417 9695441 14 20130327 0
96954417 9695441 15 20130327 0
96954417 9695441 16 20130301 0