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Remicade (Infliximab) - Death - Suspected Cause - Side Effect Reports

 
 



Index of reports > Death (600)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Remicade (Infliximab) death. The selected reports were submitted to the FDA during the sample period of about a year.

 Reports 1 - 30 of 600   Next >>

Possible Remicade side effects in male

Reported by a consumer/non-health professional from Canada on 2012-08-27

Patient: male, weighing 99.8 kg (219.5 pounds)

Reactions: Death, Gastrointestinal Haemorrhage, Drug Ineffective

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade



Possible Remicade side effects in

Reported by a physician from United Kingdom on 2012-08-23

Patient:

Reactions: Death

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade



Possible Remicade side effects in male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-23

Patient: male, weighing 62.0 kg (136.4 pounds)

Reactions: Death, Gastrointestinal Infection, Lung Neoplasm Malignant, Cystitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade

Other drugs received by patient: Lorazepam; Flovent; Solu-Cortef; Spiriva; Symbicort



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male

Reactions: Drug Ineffective, Hepatosplenic T-Cell Lymphoma, Anaemia, Sepsis, Thrombocytopenia, Leukopenia

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Azathioprine Sodium
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 1996-01-01
    End date: 2004-05-01

Azathioprine Sodium
    Dosage: variable and lower doses
    Administration route: Oral
    Start date: 2004-01-01
    End date: 2007-04-01

Humira
    Indication: Crohn's Disease
    Start date: 2007-01-01
    End date: 2007-11-01

Humira
    Start date: 2005-05-04
    End date: 2005-11-10

Remicade
    Indication: Crohn's Disease
    Start date: 2004-04-15
    End date: 2004-06-10



Possible Remicade side effects in male

Reported by a pharmacist from United States on 2012-08-21

Patient: male, weighing 74.0 kg (162.8 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma, Pancytopenia, Pyrexia, Convulsion, Mucosal Inflammation, Tumour Lysis Syndrome, Small Intestinal Ulcer Haemorrhage, Haemorrhagic Diathesis, Neutropenia

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 1997-03-25
    End date: 1997-12-01

Imuran
    Administration route: Oral
    Start date: 1999-06-14
    End date: 2002-05-22

Imuran
    Administration route: Oral
    Start date: 1997-12-01
    End date: 1999-06-13

Imuran
    Administration route: Oral
    Start date: 2001-10-25

Remicade
    Start date: 2001-12-10

Remicade
    Start date: 2001-10-24
    End date: 2001-10-24

Remicade
    Start date: 2002-05-22
    End date: 2002-05-22

Remicade
    Start date: 2001-11-08

Remicade
    Indication: Crohn's Disease
    Start date: 2002-02-25
    End date: 2002-02-25

Other drugs received by patient: Prednisone TAB; Prednisone TAB; Probiotica; Mercaptopurine; Multi-Vitamin; Iron; Budesonide; Calcium; Entocort EC; Vitamin E; Entocort EC; Macrobid



Possible Remicade side effects in male

Reported by a physician from United Kingdom on 2012-08-21

Patient: male

Reactions: Pelvic Pain, Pyrexia, Anal Fistula, C-Reactive Protein Increased, Splenomegaly, Rectal Abscess, Lethargy, Hepatosplenic T-Cell Lymphoma, Crohn's Disease, Sepsis, Platelet Count Decreased, Diabetic Ketoacidosis, Neutropenia, Rectal Discharge, Leukopenia, Influenza Like Illness

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Azathioprine Sodium
    Dosage: 2.5 mg/kg
    Indication: Crohn's Disease

Azathioprine Sodium
    Start date: 2002-01-01
    End date: 2006-09-01

Azathioprine Sodium
    Start date: 2001-06-01

Mercaptopurine
    Indication: Crohn's Disease

Prednisolone
    Indication: Product Used FOR Unknown Indication

Remicade
    Indication: Crohn's Disease
    End date: 2005-09-29

Remicade
    Dosage: stopped in february - march (3rd infusion)
    End date: 2006-02-01

Other drugs received by patient: Metronidazole; Vitamin B-12



Possible Remicade side effects in male

Reported by a pharmacist from United States on 2012-08-21

Patient: male

Reactions: Aqueductal Stenosis, Antiphospholipid Syndrome, Graft Versus Host Disease, Hepatosplenic T-Cell Lymphoma, Nuclear Magnetic Resonance Imaging Brain Abnormal, Pulmonary Embolism, Hydrocephalus, Hypertension

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Imuran
    Indication: Colitis
    Start date: 2002-11-15

Imuran
    Start date: 2001-12-01
    End date: 2002-11-14

Lovenox
    Indication: Product Used FOR Unknown Indication

Remicade
    Dosage: single infusion
    Indication: Colitis Ulcerative
    Start date: 2001-12-22
    End date: 2001-12-22

Other drugs received by patient: Asacol; Heparin; Heparin; Steroids



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male

Reactions: Multi-Organ Failure, Hepatosplenic T-Cell Lymphoma, Staphylococcal Abscess

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Mercaptopurine
    Indication: Crohn's Disease

Remicade
    Dosage: date also reported as 5-may-2005
    Start date: 2005-04-01

Remicade
    Dosage: second dose
    Indication: Crohn's Disease
    Start date: 2005-03-21

Remicade
    Start date: 2000-01-01

Other drugs received by patient: Prednisone TAB; Mesalamine



Possible Remicade side effects in 23 year old male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-21

Patient: 23 year old male

Reactions: Epstein-Barr Virus Infection, Histiocytosis Haematophagic, Hepatosplenic T-Cell Lymphoma, Septic Shock

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade

Other drugs received by patient: Mercaptopurine; Azathioprine Sodium



Possible Remicade side effects in female

Reported by a physician from United States on 2012-08-21

Patient: female, weighing 53.0 kg (116.6 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma, Neutropenic Sepsis

Adverse event resulted in: death

Drug(s) suspected as cause:
Mercaptopurine

Mercaptopurine
    Indication: Crohn's Disease

Mesalamine
    Indication: Crohn's Disease

Remicade
    Dosage: summer 2003
    Indication: Crohn's Disease
    Start date: 2001-01-15
    End date: 2003-08-15

Other drugs received by patient: Metronidazole; Hydrocortisone; Prednisone TAB



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male, weighing 115.7 kg (254.5 pounds)

Reactions: Gastrointestinal Haemorrhage, Cholecystitis Acute, T-Cell Lymphoma, Disseminated Intravascular Coagulation, Pancytopenia, Atrial Fibrillation, Multi-Organ Failure, Sepsis, Acute Respiratory Distress Syndrome

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Adriamycin PFS
    Indication: T-Cell Lymphoma
    Start date: 2006-09-10

Cyclophosphamide
    Indication: T-Cell Lymphoma
    Start date: 2006-01-01

Prednisone TAB
    Indication: T-Cell Lymphoma
    Start date: 2006-01-01

Remicade
    Dosage: 3 dose induction followed by maint. q 8 weeks, 300 mg on 29-jun-2006, total 27 infusions
    Indication: Rheumatoid Arthritis
    Start date: 2001-10-01
    End date: 2006-06-29

Vincristine
    Indication: T-Cell Lymphoma
    Start date: 2006-09-10

Other drugs received by patient: Azulfadine; Lisinopril



Possible Remicade side effects in female

Reported by a physician from Denmark on 2012-08-21

Patient: female, weighing 55.0 kg (121.0 pounds)

Reactions: Intestinal T-Cell Lymphoma

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Dosage: total of 9 infusions received
    Indication: Crohn's Disease
    Start date: 2007-01-01

Remicade
    Dosage: total of 3 infusions received
    Start date: 2008-11-28
    End date: 2009-01-08

Other drugs received by patient: Vibeden; Calcium with Vitamin D; Prednisolone; Pantoprazole Sodium; Pinex



Possible Remicade side effects in male

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-08-21

Patient: male

Reactions: Hepatosplenic T-Cell Lymphoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade

Other drugs received by patient: Pulse Steroids; Asacol; Azathioprine Sodium



Possible Remicade side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21

Patient: male, weighing 69.0 kg (151.8 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Humira
    Indication: Colitis Ulcerative
    Start date: 2007-06-15

Humira
    Start date: 2007-06-15

Humira
    Start date: 2006-11-01

Humira
    Indication: Irritable Bowel Syndrome
    Start date: 2006-11-01

Purinethol
    Dosage: also reported with start date of 01-oct-1999
    Start date: 1999-06-02

Purinethol
    Dosage: also reported with start date of 01-oct-1999
    Start date: 1999-06-02

Purinethol
    Indication: Inflammatory Bowel Disease
    End date: 2007-04-01

Purinethol
    Indication: Colitis Ulcerative
    End date: 2007-04-01

Remicade
    Dosage: 19 infusions administered between 10-jul-2002 and 7-mar-2006
    Indication: Inflammatory Bowel Disease
    Start date: 2002-07-10
    End date: 2006-03-07

Remicade
    Dosage: 19 infusions administered between 10-jul-2002 and 7-mar-2006
    Indication: Colitis Ulcerative
    Start date: 2002-07-10
    End date: 2006-03-07

Remicade
    Dosage: 19 infusions administered between 10-jul-2002 and 7-mar-2006
    Indication: Crohn's Disease
    Start date: 2002-07-10
    End date: 2006-03-07

Other drugs received by patient: Prednisone TAB; Asacol; Prednisone TAB; Asacol



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male, weighing 92.1 kg (202.6 pounds)

Reactions: T-Cell Lymphoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Mercaptopurine
    Start date: 1999-04-01

Mercaptopurine
    Indication: Crohn's Disease
    Start date: 1999-05-01
    End date: 2002-05-12

Mesalamine
    Indication: Crohn's Disease

Remicade

Remicade
    Indication: Crohn's Disease
    Start date: 1999-04-17
    End date: 1999-04-17

Other drugs received by patient: Prednisone TAB



Possible Remicade side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21

Patient: male, weighing 44.3 kg (97.5 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2000-12-01

Remicade
    Indication: Crohn's Disease
    Start date: 2002-04-01

Remicade
    Start date: 2005-10-03

Remicade
    Start date: 2003-02-05

Other drugs received by patient: Imuran; Ciprofloxacin HCL; Mercaptopurine; Pentasa



Possible Remicade side effects in male

Reported by a pharmacist from United States on 2012-08-21

Patient: male, weighing 81.7 kg (179.6 pounds)

Reactions: Neuropathy Peripheral, Lung Neoplasm, Hepatosplenic T-Cell Lymphoma, Nervous System Disorder, Muscle Rupture, Postoperative Abscess

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Mercaptopurine
    Start date: 2002-01-01

Mercaptopurine
    Indication: Crohn's Disease
    Start date: 2002-10-01

Mercaptopurine
    Dosage: decreased to 50 mg/day after 6-tg levels were found to be elevated
    Start date: 2004-01-01
    End date: 2006-08-01

Prednisone TAB
    Indication: Crohn's Disease
    Start date: 2003-08-01

Remicade
    Dosage: in 2006, the patient received 3 doses; 24 total doses over total treatment period
    Indication: Crohn's Disease
    Start date: 2002-10-01
    End date: 2006-08-01

Other drugs received by patient: Nexium; Folic Acid; Singulair; Asacol; Calcium; Nystatin; Balsalazide Disodium



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male

Reactions: Hepatosplenic T-Cell Lymphoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade
    Dosage: 5mg/kg
    Start date: 2003-03-19
    End date: 2003-03-19

Remicade
    Indication: Crohn's Disease
    Start date: 2003-04-14
    End date: 2003-04-14

Remicade
    Start date: 2003-05-28
    End date: 2003-05-28

Other drugs received by patient: Azathioprine Sodium



Possible Remicade side effects in 52 year old male

Reported by a physician from United States on 2012-08-21

Patient: 52 year old male

Reactions: Myelofibrosis, Polyp, Drug Ineffective, Hepatosplenic T-Cell Lymphoma, Neutropenic Sepsis, Myelodysplastic Syndrome, Myeloproliferative Disorder, Anaphylactoid Reaction, Polycythaemia Vera, Thrombocytopenia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Azathioprine Sodium
    Indication: Crohn's Disease
    Start date: 1989-01-01

Chop NOS
    Indication: Chemotherapy

Corticosteroid Unspecified
    Indication: Crohn's Disease

Dice (Dexamethasone,ifosfamide,cisplatin, Etoposide)
    Indication: Chemotherapy

Humira
    Indication: Crohn's Disease
    Start date: 2005-01-01

Prednisolone
    Indication: Crohn's Disease

Remicade
    Dosage: 3 total infusions
    Indication: Crohn's Disease
    Start date: 2000-01-01

Remicade
    Dosage: 1 infusion
    Start date: 2005-01-01
    End date: 2005-01-01

Tysabri
    Dosage: interval from 1st dose to the event was 7 months; 3 total doses received
    Indication: Crohn's Disease
    Start date: 2008-05-30
    End date: 2008-07-30

Other drugs received by patient: Nortriptyline; Prednisone TAB; Methadone Hydrochloride



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-21

Patient: male, weighing 81.2 kg (178.6 pounds)

Reactions: Mechanical Ventilation, Renal Failure, Hepatosplenic T-Cell Lymphoma, Sinus Disorder, Pneumothorax

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Mercaptopurine
    Administration route: Oral

Mercaptopurine
    Administration route: Oral
    Indication: Crohn's Disease

Mercaptopurine
    Administration route: Oral
    Start date: 2005-02-01

Remicade
    Dosage: started in oct or nov-2005
    Indication: Crohn's Disease
    Start date: 2005-10-01

Remicade
    Dosage: once every 6 to 7 weeks
    End date: 2007-11-20

Other drugs received by patient: Steroids NOS; Allopurinol; Ambien; Wellbutrin; Doxycycline HCL; Protonix; Bentyl; Claritin; Mesalamine; Zoloft



Possible Remicade side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-21

Patient: male, weighing 63.5 kg (139.7 pounds)

Reactions: Night Sweats, Cellulitis, Hepatosplenic T-Cell Lymphoma, Pyrexia, Thirst, Laryngitis, Leukocytoclastic Vasculitis, Epstein-Barr Virus Infection, Fatigue, Sinus Headache, Bacterial Infection, Vision Blurred, Pharyngitis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Mercaptopurine
    Dosage: 25mg am, 25mg pm
    Indication: Crohn's Disease
    Start date: 1999-11-01
    End date: 2001-02-01

Mercaptopurine
    Dosage: 25mg am, 25mg pm
    Start date: 1998-05-01

Mercaptopurine
    Dosage: 25mg am, 25mg pm
    Start date: 1997-12-01

Mercaptopurine
    Dosage: 25mg am, 25mg pm
    Start date: 1997-07-01

Remicade
    Start date: 2000-06-16

Remicade
    Start date: 2000-02-03

Remicade
    Start date: 2003-01-06

Remicade
    Start date: 2002-11-15

Remicade
    Start date: 2002-09-27

Remicade
    Start date: 1999-12-03

Remicade
    Start date: 1999-09-01

Remicade
    Start date: 2002-06-21

Remicade
    Indication: Crohn's Disease
    Start date: 2000-08-17

Remicade
    Start date: 2000-11-05

Remicade
    Start date: 2002-08-09

Remicade
    Start date: 2002-02-22

Remicade
    Start date: 2002-02-11

Other drugs received by patient: Prilosec; Azathioprine Sodium; Imuran; Prednisone TAB; Corticosteroids; Fosamax



Possible Remicade side effects in 15 year old male

Reported by a physician from United States on 2012-08-21

Patient: 15 year old male, weighing 38.3 kg (84.3 pounds)

Reactions: Respiratory Failure, Hepatosplenic T-Cell Lymphoma, Disseminated Intravascular Coagulation, Lactic Acidosis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade

Remicade

Remicade

Remicade

Remicade
    End date: 2005-06-15

Remicade
    Dosage: patient received 13 treatments.
    Start date: 2004-02-11

Remicade

Remicade

Remicade

Remicade
    Dosage: patient received 13 treatments.
    Indication: Crohn's Disease
    Start date: 2004-02-01

Remicade

Remicade

Remicade

Other drugs received by patient: Prednisone TAB; Human Growth Hormone; Imuran; Imuran; Imuran; Calcium + Vitamin D; Imuran; Imuran; Feosol; Asacol; Mercaptopurine; 5-Aminosalicylic Acid; Imuran; Imuran; Forvia; Zantac



Possible Remicade side effects in female

Reported by a physician from United States on 2012-08-21

Patient: female

Reactions: B-Cell Lymphoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade

Other drugs received by patient: Mercaptopurine



Possible Remicade side effects in male

Reported by a physician from Australia on 2012-08-21

Patient: male, weighing 120.0 kg (264.0 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma, Staphylococcal Sepsis

Adverse event resulted in: death, life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Azathioprine Sodium
    Dosage: 2-2.5 mg/kg
    Start date: 1993-01-01
    End date: 1994-01-01

Azathioprine Sodium
    Indication: Crohn's Disease
    Start date: 1999-08-01
    End date: 2006-01-01

Prednisolone
    Dosage: varying doses
    Indication: Crohn's Disease
    Start date: 1993-01-01

Remicade
    Dosage: 3 infusions
    Indication: Crohn's Disease
    Start date: 1999-11-01
    End date: 2000-01-01



Possible Remicade side effects in male

Reported by a physician from United States on 2012-08-20

Patient: male

Reactions: Meningitis Listeria

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade
    Indication: Rheumatoid Arthritis

Remicade
    Start date: 2012-07-16

Other drugs received by patient: Methotrexate



Possible Remicade side effects in female

Reported by a physician from Japan on 2012-08-20

Patient: female, weighing 47.7 kg (104.9 pounds)

Reactions: Cardio-Respiratory Arrest, Metabolic Acidosis, Hepatic Function Abnormal, Arthralgia, Disseminated Intravascular Coagulation, Platelet Count Decreased, Pyrexia, Device Related Infection, Septic Shock

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Prednisolone
    Administration route: Oral
    Indication: Rheumatoid Arthritis

Remicade
    Indication: Rheumatoid Arthritis
    Start date: 2011-12-06

Remicade
    Start date: 2010-09-03

Remicade
    Dosage: 20th dose
    Start date: 2012-06-01

Remicade
    Start date: 2009-08-21

Other drugs received by patient: Folic Acid; Edirol; Lansoprazole; Cefazolin Sodium; Warfarin Sodium



Possible Remicade side effects in 46 year old male

Reported by a physician from United Kingdom on 2012-08-20

Patient: 46 year old male

Reactions: Bronchopneumonia, Septic Shock, Leukopenia, Immunosuppression

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Dosage: 4-5 infusions
    Indication: Crohn's Disease

Remicade
    Dosage: 4th infusion
    Start date: 2011-01-11

Zometa
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-01-17

Other drugs received by patient: TPN; Prednisolone; Azathioprine Sodium



Possible Remicade side effects in female

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-20

Patient: female, weighing 59.9 kg (131.7 pounds)

Reactions: Hypovolaemic Shock, Urinary Tract Infection, Coagulopathy, Hypotension, Hepatic Enzyme Increased, Renal Failure, Sepsis Syndrome, Neuropathy Peripheral, Electrolyte Imbalance, Thrombocytopenia, Deep Vein Thrombosis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2012-03-28

Remicade
    Start date: 2012-04-26

Remicade
    Dosage: 4 vials
    Indication: Crohn's Disease
    Start date: 2012-03-14

Other drugs received by patient: Neurontin; Atarax; Protonix; Prednisone TAB; Morphine Sulfate; Prednisone TAB; Tylenol; Multivitamin; MS Contin; Rocaltrol; Vitamin D; Folic Acid; MAG-TAB; Bicarbonate; Norvasc; Celexa; Zofran; Coumadin



Possible Remicade side effects in female

Reported by a physician from United States on 2012-08-17

Patient: female, weighing 59.9 kg (131.7 pounds)

Reactions: Hypovolaemic Shock, Urinary Tract Infection, Hypotension, Coagulopathy, Hepatic Enzyme Increased, Sepsis Syndrome, Neuropathy Peripheral, Renal Failure, Electrolyte Imbalance, Thrombocytopenia, Deep Vein Thrombosis

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2012-04-26

Remicade
    Dosage: 4 vials
    Indication: Crohn's Disease
    Start date: 2012-03-14

Remicade
    Start date: 2012-03-28

Other drugs received by patient: Morphine Sulfate; Tylenol; MAG-TAB; Norvasc; Atarax; Multivitamin; Vitamin D; Zofran; Protonix; Celexa; Folic Acid; Neurontin; Bicarbonate; MS Contin; Prednisone TAB; Coumadin; Rocaltrol; Prednisone TAB



Possible Remicade side effects in female

Reported by a physician from United States on 2012-08-17

Patient: female

Reactions: Death, Aspergillosis, Lymphoma

Adverse event resulted in: death

Drug(s) suspected as cause:
Remicade



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