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
1158405411 11584054 11 F 20111012 20160708 20151001 20160722 EXP CA-VALIDUS PHARMACEUTICALS LLC-CA-2015VAL000490 VALIDUS 0.00 Y 0.00000 20160722 CN 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
1158405411 11584054 1 PS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 50 MG, BID Y 17963 50 MG
1158405411 11584054 2 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 25 MG, BID Y 17963 25 MG
1158405411 11584054 3 SS METOPROLOL TARTRATE. METOPROLOL TARTRATE 1 Oral 25 MG, QD Y 17963 25 MG
1158405411 11584054 4 SS SANDOSTATIN OCTREOTIDE ACETATE 1 Subcutaneous UNK UG, ONCE/SINGLE 0
1158405411 11584054 5 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, BIW (EVERY 2 WEEKS) U 0 40 MG
1158405411 11584054 6 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 20 MG, BIW EVERY 2 WEEKS U 0 20 MG
1158405411 11584054 7 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, BIW EVERY 2 WEEKS U S0098C 0 30 MG
1158405411 11584054 8 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 30 MG, UNK U 0 30 MG
1158405411 11584054 9 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 40 MG, BIW (EVERY 2 WEEKS) U 0 40 MG
1158405411 11584054 10 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Intramuscular 60 MG, BIW (EVERY 2 WEEKS) U 0 60 MG
1158405411 11584054 11 C LANTUS INSULIN GLARGINE 1 Subcutaneous BEDTIME 0
1158405411 11584054 12 C NOVORAPID INSULIN ASPART 1 Subcutaneous 4 TO 5 TIMES A DAY U 0
1158405411 11584054 13 C RAMIPRIL. RAMIPRIL 1 UNK U 0
1158405411 11584054 14 C CRESTOR ROSUVASTATIN CALCIUM 1 UNK U 0
1158405411 11584054 15 C ASAPHEN ASPIRIN 1 UNK U 0
1158405411 11584054 16 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U 0
1158405411 11584054 17 C GLIMEPIRIDE. GLIMEPIRIDE 1 UNK U 0
1158405411 11584054 18 C RABEPRAZOLE RABEPRAZOLE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1158405411 11584054 1 Product used for unknown indication
1158405411 11584054 4 Carcinoid syndrome
1158405411 11584054 5 Carcinoid syndrome
1158405411 11584054 11 Product used for unknown indication
1158405411 11584054 12 Product used for unknown indication
1158405411 11584054 13 Product used for unknown indication
1158405411 11584054 14 Product used for unknown indication
1158405411 11584054 15 Product used for unknown indication
1158405411 11584054 16 Product used for unknown indication
1158405411 11584054 17 Product used for unknown indication
1158405411 11584054 18 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1158405411 11584054 LT
1158405411 11584054 HO
1158405411 11584054 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
1158405411 11584054 5-hydroxyindolacetic acid in urine increased
1158405411 11584054 Abdominal discomfort
1158405411 11584054 Abdominal distension
1158405411 11584054 Abdominal mass
1158405411 11584054 Abdominal pain
1158405411 11584054 Abdominal pain upper
1158405411 11584054 Arthralgia
1158405411 11584054 Asthenia
1158405411 11584054 Blood chromogranin A increased
1158405411 11584054 Blood glucose decreased
1158405411 11584054 Blood glucose fluctuation
1158405411 11584054 Blood pressure diastolic decreased
1158405411 11584054 Blood pressure systolic increased
1158405411 11584054 Diabetes mellitus
1158405411 11584054 Diarrhoea
1158405411 11584054 Discomfort
1158405411 11584054 Disorientation
1158405411 11584054 Dyspnoea
1158405411 11584054 Fatigue
1158405411 11584054 Feeling abnormal
1158405411 11584054 Flushing
1158405411 11584054 Frequent bowel movements
1158405411 11584054 Gait disturbance
1158405411 11584054 Gastrointestinal hypomotility
1158405411 11584054 Heart rate decreased
1158405411 11584054 Hyperhidrosis
1158405411 11584054 Hypotension
1158405411 11584054 Inappropriate schedule of drug administration
1158405411 11584054 Incorrect dose administered
1158405411 11584054 Injection site bruising
1158405411 11584054 Injection site discomfort
1158405411 11584054 Injection site mass
1158405411 11584054 Injection site pain
1158405411 11584054 Injection site scar
1158405411 11584054 Macular degeneration
1158405411 11584054 Malignant neoplasm progression
1158405411 11584054 Nausea
1158405411 11584054 Needle issue
1158405411 11584054 Oncologic complication
1158405411 11584054 Sleep disorder
1158405411 11584054 Syncope
1158405411 11584054 Therapeutic response decreased
1158405411 11584054 Underdose
1158405411 11584054 Visual acuity reduced
1158405411 11584054 Visual impairment

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
1158405411 11584054 4 20110927 20110927 0
1158405411 11584054 5 20111012 0
1158405411 11584054 7 20110927 0
1158405411 11584054 8 20140606 0