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Celebrex (Celecoxib) - Adverse Event Reports - Hospitalization - Cardiac Failure Congestive

 



Index of reports > Cases resulting in hospitalization (1821) > Cases with Cardiac Failure Congestive (93)

Below is the selection of adverse event reports related to Celebrex (Celecoxib) that includes cases resulting in hospitalization where reactions include cardiac failure congestive.

 Reports 1 - 25 of 93   Next >>

Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-18

Patient: female

Adverse reactions / side effects: Systemic Lupus Erythematosus, Coronary Artery Occlusion, Depression, Cardiac Failure Congestive

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-16

Patient: female, weighing 95.3 kg (209.7 pounds)

Adverse reactions / side effects: Myocardial Infarction, Cardiovascular Disorder, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Administration route: Oral
    Indication: Osteoarthritis

Celebrex
    Indication: Pain

Vioxx
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2000-08-09



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-16

Patient: female, weighing 75.8 kg (166.8 pounds)

Adverse reactions / side effects: Myocardial Infarction, Cardiovascular Disorder, Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Bextra
    Indication: Pain
    Start date: 2002-04-02
    End date: 2004-08-22

Celebrex
    Dosage: freq:frequency: 1-2
    Indication: Pain
    Start date: 2002-09-01
    End date: 2004-08-22

Vioxx
    Indication: Arthralgia
    Start date: 2001-09-02
    End date: 2004-08-22

Other drugs received by patient: Acetaminophen; Cyclobenzaprine HCL; Lotensin; Enalapril Maleate; Coreg; Coreg; Minitran; Minitran; Digoxin; Digitek; Coumadin; Hydrocodone; Levothyroxine Sodium; Levoxyl; Synthroid



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-16

Patient: female, weighing 86.2 kg (189.6 pounds)

Adverse reactions / side effects: Coronary Artery Disease, Cardiovascular Disorder, Cerebrovascular Accident, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Administration route: Oral
    Indication: Pain

Celebrex
    Indication: Osteoarthritis

Vioxx
    Dosage: text:12.5mg and 25mg
    Administration route: Oral
    Indication: Pain
    Start date: 1999-08-30

Vioxx
    Indication: Osteoarthritis

Other drugs received by patient: Hydrocodone; Aspirin



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-15

Patient: female

Adverse reactions / side effects: Cardiovascular Disorder, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Administration route: Oral
    Indication: Arthralgia
    Start date: 1999-03-01
    End date: 2001-11-01

Celebrex
    Indication: Osteoarthritis

Vioxx
    Administration route: Oral
    Indication: Arthralgia
    Start date: 2001-11-01

Vioxx
    Indication: Osteoarthritis

Other drugs received by patient: Vicodin; Amitriptyline HCL; Cozaar; Cozaar; Cardizem; Cardizem; Lasix; Plavix; Prempro; Theophylline; K-DUR 10



Adverse event in male receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-11

Patient: male, weighing 105.7 kg (232.5 pounds)

Adverse reactions / side effects: Thrombosis, Pulmonary Embolism, Cerebrovascular Accident, Arrhythmia, Organ Failure, Memory Impairment, Depression, Myocardial Infarction, Cardiac Failure Congestive, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Bextra
    Administration route: Oral
    Indication: Pain

Celebrex
    Administration route: Oral
    Indication: Pain
    Start date: 1999-01-01

Other drugs received by patient: Vioxx



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-10-11

Patient: female, weighing 71.2 kg (156.6 pounds)

Adverse reactions / side effects: Pulmonary Embolism, Cardiovascular Disorder, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Bextra
    Indication: Back Pain
    Start date: 2003-01-01

Celebrex
    Indication: Pain
    Start date: 2002-01-01
    End date: 2002-12-01

Vioxx
    Administration route: Oral
    Indication: Back Pain



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-27

Patient: female, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Myocardial Infarction, Cardiovascular Disorder, Cardiac Failure Congestive

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Celebrex
    Indication: Arthritis

Vioxx
    Indication: Carpal Tunnel Syndrome
    Start date: 2000-02-25
    End date: 2001-08-24

Vioxx
    Indication: Arthritis

Other drugs received by patient: Zocor; Percocet; Oxycodone HCL



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-27

Patient: female, weighing 57.6 kg (126.7 pounds)

Adverse reactions / side effects: Pulmonary Embolism, Cardiovascular Disorder, Cardiac Failure Congestive, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Administration route: Oral
    Indication: Arthritis

Vioxx
    Administration route: Oral
    Indication: Arthritis
    Start date: 2000-10-09

Other drugs received by patient: Acetaminophen W / Codeine; Cyclobenzaprine HCL; Imitrex; Methylprednisolone



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-27

Patient: female, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Arthralgia, Oedema Peripheral, Reproductive Tract Disorder, Vision Blurred, Depression, Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Bextra
    Indication: Arthralgia

Celebrex
    Indication: Arthralgia

Celebrex
    Indication: Pain

Vioxx
    Indication: Arthralgia
    Start date: 2002-12-10
    End date: 2004-09-30

Other drugs received by patient: Prevacid; Ibuprofen



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a consumer/non-health professional from United States on 2007-07-25

Patient: female

Adverse reactions / side effects: Renal Disorder, Blood Potassium Decreased, Urosepsis, Asthenia, Blood Creatinine Increased, Cardiac Failure Congestive, Hepatocellular Damage

Adverse event resulted in: hospitalization

Suspect drug(s):
ALL Other Therapeutic Products
    Indication: Urosepsis

Celebrex
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2004-12-01
    End date: 2005-10-01

Other drugs received by patient: Synthroid; Atenolol; Avalide; Tylenol (Caplet); ALL Other Therapeutic Products; Bumex



Adverse event in male receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-24

Patient: male

Adverse reactions / side effects: Anger, Depression, Amnesia, Chronic Obstructive Pulmonary Disease, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Indication: Back Injury

Celebrex
    Indication: Arthritis



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-24

Patient: female, weighing 76.2 kg (167.6 pounds)

Adverse reactions / side effects: Myocardial Infarction, Acute Coronary Syndrome, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Bextra
    Indication: Arthritis
    Start date: 2001-11-01
    End date: 2004-09-30

Celebrex
    Indication: Arthritis
    Start date: 1999-01-01
    End date: 2004-09-30

Vioxx
    Start date: 2001-08-18
    End date: 2004-09-01

Other drugs received by patient: Tylenol W / Codeine; Hydrocodone Bitartrate + Acetaminophen; Quinine Sulfate; Tylenol W / Codeine NO. 3; Levoxyl



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-24

Patient: female

Adverse reactions / side effects: Diabetes Mellitus, Condition Aggravated, Depression, LEG Amputation, Hypertension, TOE Amputation, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-24

Patient: female, weighing 61.2 kg (134.6 pounds)

Adverse reactions / side effects: Thrombosis, Pulmonary Embolism, Myocardial Infarction, Cardiac Failure Congestive, Deep Vein Thrombosis

Adverse event resulted in: death, hospitalization, disablity

Suspect drug(s):
Celebrex
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2002-02-25
    End date: 2004-04-04

Vioxx
    Administration route: Oral
    Start date: 2002-12-01
    End date: 2004-02-01



Adverse event in male receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-24

Patient: male

Adverse reactions / side effects: Cardiac Murmur, Paralysis, Blindness Unilateral, Amnesia, Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Bextra
    Administration route: Oral

Celebrex
    Administration route: Oral

Vioxx
    Administration route: Oral



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-23

Patient: female, weighing 65.8 kg (144.8 pounds)

Adverse reactions / side effects: Rash, Cerebrovascular Accident, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Bextra

Celebrex
    Indication: Arthritis



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a lawyer from United States on 2007-07-19

Patient: female

Adverse reactions / side effects: Myocardial Infarction, Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Bextra
    Indication: Pain
    Start date: 2001-11-01
    End date: 2004-05-18

Celebrex
    Indication: Pain
    Start date: 1999-01-01
    End date: 2004-05-18

Vioxx
    Administration route: Oral
    Start date: 2000-01-01
    End date: 2004-05-18



Adverse event in 67 year old female receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: 67 year old female, weighing 81.6 kg (179.5 pounds)

Adverse reactions / side effects: Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Bextra
    Dosage: 20 mg (20 mg,1 in 1 d),oral
    Administration route: Oral
    Indication: Back Pain
    Start date: 2003-06-13

Bextra
    Dosage: 20 mg (20 mg,1 in 1 d),oral
    Administration route: Oral
    Indication: Pain in Extremity
    Start date: 2003-06-13

Celebrex
    Dosage: 400 mg (200 mg,2 in 1 d),oral
    Administration route: Oral
    Indication: Back Pain
    Start date: 1999-07-21

Celebrex
    Dosage: 400 mg (200 mg,2 in 1 d),oral
    Administration route: Oral
    Indication: Pain in Extremity
    Start date: 1999-07-21



Adverse event in 41 year old female receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: 41 year old female

Adverse reactions / side effects: Pulmonary Embolism, Cerebrovascular Accident, Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in 73 year old male receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: 73 year old male

Adverse reactions / side effects: Myocardial Infarction, Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: female

Adverse reactions / side effects: Myocardial Infarction, Cardiac Failure Congestive, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Dosage: 400 mg (200 mg, 2 in 1 d)
    Indication: Pain
    Start date: 2002-01-01

Vioxx
    Start date: 1999-10-01



Adverse event in 70 year old male receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: 70 year old male

Adverse reactions / side effects: Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in 76 year old male receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: 76 year old male, weighing 82.6 kg (181.7 pounds)

Adverse reactions / side effects: Cerebrovascular Accident, Cardiac Failure Congestive

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Celebrex (Celecoxib)



Adverse event in female receiving Celebrex (Celecoxib)

Reported by a individual with unspecified qualification from United States on 2007-07-18

Patient: female

Adverse reactions / side effects: Myocardial Infarction, Cardiac Failure Congestive

Adverse event resulted in: hospitalization

Suspect drug(s):
Celebrex
    Dosage: 200 mg (200 mg , 1 in 1 d), oral
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2001-07-27

Vioxx
    Dosage: oral
    Administration route: Oral
    Start date: 1999-05-20
    End date: 2001-01-14



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