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
125377191 12537719 1 I 20131107 20151016 20160707 20160707 EXP CA-VALIDUS PHARMACEUTICALS LLC-CA-2015VAL000672 VALIDUS 0.00 Y 0.00000 20160707 MD 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
125377191 12537719 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 UNK U 17963
125377191 12537719 2 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular 20 MG, QMO (EVERY 4 WEEKS) Y 0 20 MG
125377191 12537719 3 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Intramuscular 30 MG, QMO (EVERY 4 WEEKS) Y 0 30 MG
125377191 12537719 4 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous UNK, BID FOR 6 WEEKS U 0
125377191 12537719 5 C RANITIDINE. RANITIDINE 1 UNK U 0
125377191 12537719 6 C LYRICA PREGABALIN 1 UNK U 0
125377191 12537719 7 C NORVASC AMLODIPINE BESYLATE 1 UNK U 0
125377191 12537719 8 C ASPIRIN /00002701/ ASPIRIN 1 UNK U 0
125377191 12537719 9 C COGENTIN BENZTROPINE MESYLATE 1 UNK U 0
125377191 12537719 10 C IRON IRON 1 UNK U 0
125377191 12537719 11 C MEXIRAN 2 UNK U 0
125377191 12537719 12 C PLAVIX CLOPIDOGREL BISULFATE 1 UNK U 0
125377191 12537719 13 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK U 0
125377191 12537719 14 C MODECATE FLUPHENAZINE DECANOATE 1 UNK U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125377191 12537719 1 Product used for unknown indication
125377191 12537719 2 Metastatic carcinoid tumour
125377191 12537719 4 Product used for unknown indication
125377191 12537719 5 Product used for unknown indication
125377191 12537719 6 Product used for unknown indication
125377191 12537719 7 Product used for unknown indication
125377191 12537719 8 Product used for unknown indication
125377191 12537719 9 Product used for unknown indication
125377191 12537719 10 Product used for unknown indication
125377191 12537719 11 Product used for unknown indication
125377191 12537719 12 Product used for unknown indication
125377191 12537719 13 Product used for unknown indication
125377191 12537719 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125377191 12537719 DE
125377191 12537719 HO
125377191 12537719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125377191 12537719 Abscess
125377191 12537719 Blood pressure increased
125377191 12537719 Blood pressure systolic increased
125377191 12537719 Death
125377191 12537719 Decreased appetite
125377191 12537719 Diarrhoea
125377191 12537719 Fall
125377191 12537719 Fatigue
125377191 12537719 Flatulence
125377191 12537719 Full blood count decreased
125377191 12537719 Gastric cancer
125377191 12537719 Haemoglobin decreased
125377191 12537719 Influenza
125377191 12537719 Malaise
125377191 12537719 Malignant neoplasm progression
125377191 12537719 Metastases to liver
125377191 12537719 Muscle spasms
125377191 12537719 Nasopharyngitis
125377191 12537719 Neoplasm
125377191 12537719 Post procedural infection
125377191 12537719 Respiratory tract infection
125377191 12537719 Second primary malignancy
125377191 12537719 Sleep disorder
125377191 12537719 Vomiting
125377191 12537719 Weight decreased
125377191 12537719 Wheezing

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
125377191 12537719 2 20101018 0
125377191 12537719 4 20100920 0