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
125378402 12537840 2 F 20160706 20160707 20160720 EXP AU-VALIDUS PHARMACEUTICALS LLC-AU-2016VAL002202 VALIDUS 0.00 Y 0.00000 20160720 MD AU AU

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
125378402 12537840 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Unknown 12.5 MG, UNK U 17963 12.5 MG
125378402 12537840 2 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 U 17963
125378402 12537840 3 SS GALVUMET METFORMIN HYDROCHLORIDEVILDAGLIPTIN 1 UNK U 0
125378402 12537840 4 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK U 0
125378402 12537840 5 C LATUDA LURASIDONE HYDROCHLORIDE 1 UNK U 0
125378402 12537840 6 C SEROQUEL QUETIAPINE FUMARATE 1 UNK U 0
125378402 12537840 7 C EPILIM VALPROATE SODIUM 1 UNK U 0
125378402 12537840 8 C ROSUVASTATIN. ROSUVASTATIN 1 UNK U 0
125378402 12537840 9 C EUTROXSIG LEVOTHYROXINE SODIUM 1 UNK U 0
125378402 12537840 10 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 UNK U 0 INHALER
125378402 12537840 11 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 UNK U 0
125378402 12537840 12 C ASPIRIN /00346701/ ASCORBIC ACIDASPIRIN 1 UNK U 0
125378402 12537840 13 C VITAMINS WITH MINERALS MINERALSVITAMINS 1 UNK U 0
125378402 12537840 14 C VITAMIN D3 CHOLECALCIFEROL 1 UNK U 0
125378402 12537840 15 C COD LIVER OIL COD LIVER OIL 1 UNK U 0
125378402 12537840 16 C PANADOL ACETAMINOPHEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125378402 12537840 1 Cardiac disorder
125378402 12537840 2 Hypertension
125378402 12537840 3 Product used for unknown indication
125378402 12537840 4 Product used for unknown indication
125378402 12537840 5 Product used for unknown indication
125378402 12537840 6 Product used for unknown indication
125378402 12537840 7 Product used for unknown indication
125378402 12537840 8 Product used for unknown indication
125378402 12537840 9 Product used for unknown indication
125378402 12537840 10 Product used for unknown indication
125378402 12537840 11 Product used for unknown indication
125378402 12537840 12 Product used for unknown indication
125378402 12537840 13 Product used for unknown indication
125378402 12537840 14 Product used for unknown indication
125378402 12537840 15 Product used for unknown indication
125378402 12537840 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125378402 12537840 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125378402 12537840 Acute coronary syndrome
125378402 12537840 Asthenia
125378402 12537840 Blood pressure increased
125378402 12537840 Chest pain
125378402 12537840 Cognitive disorder
125378402 12537840 Coronary artery disease
125378402 12537840 Coronary artery stenosis
125378402 12537840 Dyspnoea
125378402 12537840 Emphysema
125378402 12537840 Osteoarthritis
125378402 12537840 Schizophrenia
125378402 12537840 Sleep apnoea syndrome
125378402 12537840 Type 2 diabetes mellitus

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

no results found

Therapies reported

no results found