Bextra and condition aggravated Patient Reports February 11, 2012

Bextra Side Effects Report #4648649-5
Bextra side effect was reported by a Consumer or non-health professional from on Apr 15, 2005. Male patient, 35 years of age, was diagnosed with tendonitis and was treated with Bextra. After drug was administered, patient experienced the following side effects: asthma , condition aggravated. Bextra dosage: 40 MG, ORAL. Patient recovered.

Bextra Side Effects Report #5423020-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 10, 2007. Female patient, weighting 145.5 lb, was diagnosed with systemic lupus erythematosus, arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: accident, blood pressure increased, condition aggravated, muscle injury, muscle operation, panic attack, skin haemorrhage, systemic lupus erythematosus. Bextra dosage: unknown. During the same period patient was treated with ANALGESICS, ACCUPRIL, SPIRONOLACTONE, NORTRIPTYLINE, DICYCLOMINE, TRIAMTERENE AND HYDROCHLOROTHIAZIDE. Patient died.

Bextra Side Effects Report #4646635-2
Bextra side effect was reported by a Consumer or non-health professional from on Feb 17, 2005. Male patient, 58 years of age, weighting 170.0 lb, was diagnosed with spondylitis, blood cholesterol increased and was treated with Bextra. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, condition aggravated, fall , headache , intentional self-injury, laceration, myalgia, neck pain. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LIPITOR, CLONAZEPAM, ESCITALOPRAM OXALATE, LAMOTRIGINE, METHYLPHENIDATE, EZETIMIBE. Patient recovered.

Bextra Side Effects Report #4655531-6
Bextra side effect was reported by a Physician from on Apr 25, 2005. Male patient, 58 years of age, weighting 170.0 lb, was diagnosed with spondylitis, blood cholesterol increased and was treated with Bextra. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, condition aggravated, fall , headache , myalgia, neck pain, suicide attempt. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LIPITOR, CLONAZEPAM, ESCITALOPRAM OXALATE, LAMOTRIGINE, METHYLPHENIDATE, EZETIMIBE. Patient recovered.


Bextra Side Effects Report #4717253-2
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 04, 2005. Male patient, 58 years of age, was diagnosed with scrotal disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, furuncle, genital injury, hypertension, musculoskeletal stiffness, neck pain. Bextra dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ANTIHYPERTENSIVES, ENALAPRIL. Patient recovered.

Bextra Side Effects Report #5095020-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 16, 2006. Male patient, 71 years of age, weighting 190.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, cerebrovascular accident, condition aggravated, confusional state, mental disorder, myocardial infarction. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient died on 09/26/2003.

Bextra Side Effects Report #4980857-6
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 06, 2005. Female patient, 67 years of age, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: anorexia, arthralgia, asthenia, cardiac failure congestive, condition aggravated, conjunctivitis, culture urine positive, endocarditis bacterial, extradural abscess. Bextra dosage: unknown. During the same period patient was treated with METHOTREXATE, KENALOG. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4655869-2
Bextra side effect was reported by a Physician from on Apr 22, 2005. Female patient, 62 years of age, was diagnosed with rheumatoid arthritis , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, neutropenia. Bextra dosage: 10 MG (1 D),. During the same period patient was treated with NAPROXEN. Patient recovered.

Bextra Side Effects Report #4737403-1
Bextra side effect was reported by a Health Professional from UNITED STATES on July 25, 2005. Female patient, 62 years of age, weighting 205.0 lb, was diagnosed with rheumatoid arthritis , psoriasis and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, blood pressure abnormal, bronchitis , chronic obstructive pulmonary disease, condition aggravated, diabetes mellitus, diabetes mellitus non-insulin-dependent, fatigue. Bextra dosage: 20 MG (20 MG, 2 IN 1 D), ORAL. During the same period patient was treated with METHOTREXATE, ETANERCEPT, PROTOPIC, KERALYT, LOTREL, THEOPHYLLINE, ADVAIR. Patient recovered.


Bextra Side Effects Report #4789642-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 21, 2005. Male patient, 62 years of age, weighting 310.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: angina pectoris, cardiac disorder, cardiomegaly, condition aggravated, pneumonia , pollakiuria, renal failure, renal pain. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, VIOXX, NAPROSYN, INSULIN, COREG. Patient recovered.

Bextra Side Effects Report #4802411-9
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 29, 2005. Male patient, 62 years of age, weighting 310.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: abdominal pain , angina pectoris, blister, cardiac disorder, cardiomegaly, condition aggravated, dyspepsia, headache , lung disorder. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, VIOXX, NAPROSYN, INSULIN, COREG. Patient recovered.

Bextra Side Effects Report #4595178-3
Bextra side effect was reported by a Consumer or non-health professional from on Feb 10, 2005. Male patient, 61 years of age, weighting 310.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: angina pectoris, cardiomegaly, condition aggravated, pneumonia , pollakiuria, renal failure, renal pain. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, ROFECOXIB, NAPROXEN, INSULIN, CARVEDILOL. Patient recovered.

Bextra Side Effects Report #5074911-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 14, 2006. Male patient, 55 years of age, weighting 190.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , cerebrovascular accident, condition aggravated, depression , myocardial infarction. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4696330-9
Bextra side effect was reported by a Consumer or non-health professional from on June 07, 2005. Male patient, 54 years of age, weighting 208.0 lb, was diagnosed with rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, cardiac disorder, chest discomfort, chest pain , coma, condition aggravated, dyspnoea exertional, pain in extremity. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ALLOPURINOL, NAPROXEN, HYDROCODONE BITARTRATE. Patient recovered.


Bextra Side Effects Report #4701785-7
Bextra side effect was reported by a Consumer or non-health professional from on June 13, 2005. Male patient, 54 years of age, weighting 208.0 lb, was diagnosed with rheumatoid arthritis , gout  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, chest discomfort, chest pain , coma, condition aggravated, dyspnoea, feeling hot, rheumatoid arthritis . Bextra dosage: 10 MG (10 MG 1 IN 1 D)ORAL. During the same period patient was treated with ALLOPURINOL, NAPROXEN, HYDROCODONE. Patient recovered.

Bextra Side Effects Report #4863236-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2005. Male patient, weighting 205.0 lb, was diagnosed with rheumatoid arthritis , erectile dysfunction  and was treated with Bextra. After drug was administered, patient experienced the following side effects: blood pressure decreased, blood pressure increased, bronchitis , condition aggravated, dehydration, erectile dysfunction , gastric ulcer, headache . Bextra dosage: unknown. During the same period patient was treated with VIAGRA, VIOXX, CIALIS, LEVITRA. Patient recovered.

Bextra Side Effects Report #4717288-X
Bextra side effect was reported by a Consumer or non-health professional from BRAZIL on July 04, 2005. Female patient, 27 years of age, was diagnosed with procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, dermatitis allergic, gastric disorder, pregnancy . Bextra dosage: unknown. Patient recovered.

Bextra Side Effects Report #4587432-6
Bextra side effect was reported by a Consumer or non-health professional from on Feb 02, 2005. Male patient, 37 years of age, was diagnosed with post procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, duodenitis, dyspepsia, dysphagia, gastritis, oesophageal ulcer, pain . Bextra dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with DICLOFENAC, DOXYCYCLINE, RABEPRAZOLE. Patient recovered.

Bextra Side Effects Report #4649860-X
Bextra side effect was reported by a Consumer or non-health professional from on Apr 15, 2005. Female patient, 27 years of age, was diagnosed with post procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, dermatitis allergic. Bextra dosage: unknown. Patient recovered.


Bextra Side Effects Report #4687230-9
Bextra side effect was reported by a Consumer or non-health professional from on May 23, 2005. Female patient, 27 years of age, was diagnosed with post procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: blister, condition aggravated, dermatitis allergic, gastric disorder, skin exfoliation. Bextra dosage: unknown. Patient recovered.

Bextra Side Effects Report #4690491-3
Bextra side effect was reported by a Consumer or non-health professional from on June 06, 2005. Female patient, 27 years of age, was diagnosed with post procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: blister, condition aggravated, dermatitis allergic, gastric disorder, skin exfoliation. Bextra dosage: unknown. Patient recovered.

Bextra Side Effects Report #4603352-2
Bextra side effect was reported by a Consumer or non-health professional from on Feb 23, 2005. Male patient was diagnosed with post procedural pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, duodenitis, dyspepsia, dysphagia, gastritis, oesophageal ulcer, pain . Bextra dosage: 40 MG (40 MG, SINGLE INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with DICLOFENAC, DOXYCYCLINE, RABEPRAZOLE, PANTOPRAZOLE. Patient recovered.

Bextra Side Effects Report #4589558-X
Bextra side effect was reported by a Physician from on Feb 02, 2005. Male patient, 65 years of age, weighting 207.2 lb, was diagnosed with polyarthritis, psoriasis and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac failure, cardiomegaly, condition aggravated, dyspnoea, emphysema, fatigue, obstructive airways disorder, procedural complication, pulmonary congestion. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ASPIRIN, ISOSORBIDE DINITRATE, MOLSIDOMINE, LISINOPRIL, BISOPROLOL FUMARATE, LEVOTHYROXINE, INSUMAN. Patient recovered.

Bextra Side Effects Report #4650422-9
Bextra side effect was reported by a Consumer or non-health professional from on Apr 16, 2005. Female patient, 78 years of age, was diagnosed with pain in extremity and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, difficulty in walking, erythema, varicose vein . Bextra dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient recovered.


Bextra Side Effects Report #4692253-X
Bextra side effect was reported by a Consumer or non-health professional from on June 01, 2005. Female patient, 78 years of age, was diagnosed with pain in extremity and was treated with Bextra. After drug was administered, patient experienced the following side effects: angiopathy, condition aggravated, difficulty in walking, erythema, pain in extremity, varicose vein . Bextra dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient recovered.

Bextra Side Effects Report #4625906-X
Bextra side effect was reported by a Consumer or non-health professional from on Mar 15, 2005. Male patient, 72 years of age, weighting 150.0 lb, was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, heart rate decreased, muscle strain, pain . Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with METFORMIN, GLYBURIDE, PROPRANOLOL. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4693988-5
Bextra side effect was reported by a Consumer or non-health professional from on June 03, 2005. Female patient, 70 years of age, weighting 200.0 lb, was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, difficulty in walking, feeling abnormal, limb operation, pain , trigger finger, wrist surgery. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PROTONIX, ANTIHYPERTENSIVES, ZOCOR, INSULIN, AVANDAMET. Patient recovered.

Bextra Side Effects Report #5075757-X
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2006. Female patient, 61 years of age, was diagnosed with pain , depression , trigeminal neuralgia  and was treated with Bextra. After drug was administered, patient experienced the following side effects: balance disorder, condition aggravated, confusional state, contusion, dizziness , endodontic procedure, hot flush, hunger, malaise. Bextra dosage: unknown. During the same period patient was treated with ZOLOFT, CELEBREX, LYRICA, TEGRETOL, THYROID, FOSAMAX. Patient recovered.

Bextra Side Effects Report #4603752-0
Bextra side effect was reported by a Consumer or non-health professional from on Nov 04, 2004. Male patient, 58 years of age, weighting 190.0 lb, was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, chest pain , condition aggravated, dizziness , dyspnoea, pruritus, rash pruritic, skin irritation. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with VICODIN, TEMAZEPAM, INSULIN, ATENOLOL, LISINOPRIL, PROPRANOLOL HYDROCHLORIDE, CLOPIDOGREL BISULPHATE. Patient was hospitalized. Patient recovered.


Bextra Side Effects Report #4903651-0
Bextra side effect was reported by a Physician from UNITED STATES on Jan 23, 2006. Female patient, 55 years of age, weighting 135.0 lb, was diagnosed with pain , scleroderma , joint swelling and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, difficulty in walking, hypertension, joint swelling, lung operation, oedema peripheral, oesophageal dilatation. Bextra dosage: unknown. During the same period patient was treated with CELEBREX, PREDNISONE, NEXIUM, ANTIHYPERTENSIVES, IMITREX, NAPROSYN. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4660994-6
Bextra side effect was reported by a Consumer or non-health professional from on May 02, 2005. Female patient, 53 years of age, weighting 138.0 lb, was diagnosed with pain , rheumatoid arthritis , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: blood pressure decreased, blood pressure increased, chest discomfort, chest pain , condition aggravated, flushing, hypertension. Bextra dosage: 20 MG (10 MG, 2 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, PROVELLA, PREDNISONE, CETIRIZINE, ENDAL, FLUNISOLIDE, MOMETASONE FUROATE. Patient recovered.

Bextra Side Effects Report #4967120-4
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2006. Female patient, 52 years of age, was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, haemodialysis, renal failure. Bextra dosage: 20 MG (1 IN 1 D), ORAL. During the same period patient was treated with VICODIN, ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5273095-3
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2007. Male patient, weighting 274.9 lb, was diagnosed with pain , inflammation, back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: anxiety , arteriosclerosis, atrial fibrillation , cardiomyopathy , condition aggravated, depression , hypertension, myocardial infarction, nephrolithiasis. Bextra dosage: unknown. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5132027-9
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2006. Male patient, weighting 164.0 lb, was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: amnesia, cardiac disorder, cerebrovascular accident, cerebrovascular disorder, condition aggravated, confusional state, dementia , hypertension, injury. Bextra dosage: 10 MG (10 MG, 1 IN 1 D). Patient was hospitalized. Patient died on 07/09/2006.


Bextra Side Effects Report #4819867-8
Bextra side effect was reported by a Pharmacist from BRAZIL on Oct 20, 2005. Male patient was diagnosed with pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, diabetes mellitus, infarction. Bextra dosage: (40 MG), ORAL. Patient died.

Bextra Side Effects Report #4673016-8
Bextra side effect was reported by a Physician from on May 09, 2005. Female patient, 86 years of age, weighting 176.4 lb, was diagnosed with osteoarthritis , neuropathic pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac failure, condition aggravated, incorrect dose administered. Bextra dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LYRICA, METHENAMINE HIPPURATE, ZOPICLONE, LANSOPRAZOLE, WARFARIN, SERETIDE MITE, PERINDOPRIL, AMITRIPTYLINE HYDROCHLORIDE. Patient died on 04/06/2005.

Bextra Side Effects Report #4673726-2
Bextra side effect was reported by a Physician from on May 10, 2005. Female patient, 84 years of age, weighting 165.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthropathy, condition aggravated, movement disorder , pain , pain in extremity. Bextra dosage: 10 MG (10 MG, 1 IN 1 D) ORAL. During the same period patient was treated with TENORMIN, SYNTHROID, PREVACID. Patient recovered.

Bextra Side Effects Report #4704735-2
Bextra side effect was reported by a Physician from on June 17, 2005. Female patient, 84 years of age, weighting 165.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, dysgraphia, knee arthroplasty, mass, pain , pain in extremity. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TENORMIN, SYNTHROID, PREVACID. Patient recovered.

Bextra Side Effects Report #4588896-4
Bextra side effect was reported by a Consumer or non-health professional from on Feb 02, 2005. Female patient, 82 years of age, weighting 183.0 lb, was diagnosed with osteoarthritis , rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , condition aggravated, diverticulitis, gallbladder operation, gastrointestinal disorder, pancreatitis. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PREDNISONE, CORTISONE, ULTRACET. Patient was hospitalized. Patient recovered.


Bextra Side Effects Report #4676782-0
Bextra side effect was reported by a Health Professional from on Feb 15, 2005. Female patient, 70 years of age, weighting 142.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: angina pectoris, back pain , blood potassium decreased, bundle branch block right, condition aggravated, cyanosis, feeling abnormal, heart rate irregular. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, SYNTHROID, FOSAMAX, MAXZIDE, NORVASC. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4823978-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 24, 2005. Female patient, 65 years of age, weighting 210.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, osteoarthritis , walking aid user. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). During the same period patient was treated with ASPIRIN. Patient recovered.

Bextra Side Effects Report #4882493-9
Bextra side effect was reported by a Health Professional from UNITED STATES on Jan 04, 2006. Female patient, 65 years of age, weighting 210.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, arthritis , condition aggravated. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). During the same period patient was treated with ASPIRIN. Patient recovered.

Bextra Side Effects Report #4650867-7
Bextra side effect was reported by a Consumer or non-health professional from on Apr 18, 2005. Female patient, 60 years of age, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, erythema, gastrooesophageal reflux disease, headache , memory impairment, pain , panic attack, skin discolouration, skin exfoliation. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, FUROSEMIDE, ENALAPRIL MALEATE, MIRTAZAPINE, ALPRAZOLAM, FLUOXETINE, FISH OIL, OMEPRAZOLE. Patient recovered.

Bextra Side Effects Report #5192684-8
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 11, 2006. Male patient, 59 years of age, weighting 330.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: amnesia, cardiogenic shock, condition aggravated, deep vein thrombosis , osteoarthritis , pulmonary embolism . Bextra dosage: 40 MG (20 MG, 2 IN 1 D). Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5074870-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 24, 2006. Male patient, 56 years of age, weighting 269.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, coronary artery disease . Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient recovered.

Bextra Side Effects Report #4594756-5
Bextra side effect was reported by a Consumer or non-health professional from on Feb 09, 2005. Female patient, 40 years of age, weighting 178.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: alopecia, cervicectomy, condition aggravated, polycystic ovaries. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MORPHINE, GABAPENTIN, ESTRADIOL, METFORMIN, GUAIFENESIN, CITALOPRAM HYDROBROMIDE, VENLAFAXINE, TOPIRAMATE. Patient recovered.

Bextra Side Effects Report #4602370-8
Bextra side effect was reported by a Consumer or non-health professional from on Feb 18, 2005. Female patient, 40 years of age, weighting 178.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: alopecia, condition aggravated, hysterectomy , polycystic ovaries. Bextra dosage: 20 MG (20 MG, 1 IN 1 D),ORAL. During the same period patient was treated with MORPHINE, GABAPENTIN, ESTRADIOL, METFORMIN, GUAIFENESIN, CITALOPRAM HYDROBROMIDE, VENLAFAXINE, TOPIRAMATE. Patient recovered.

Bextra Side Effects Report #4660996-X
Bextra side effect was reported by a Consumer or non-health professional from on Apr 28, 2005. Female patient, weighting 190.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, arthropathy, asthma , condition aggravated, dry skin, dysphagia, fatigue, gastrooesophageal reflux disease, hypothyroidism. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CALCIUM, VITAMIN E, LIPITOR. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4715443-6
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on June 30, 2005. Female patient, weighting 165.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, condition aggravated, dysgraphia, mass, pain , pain in extremity, treatment noncompliance. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TENORMIN, SYNTHROID, PREVACID. Patient recovered.


Bextra Side Effects Report #4729426-3
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 14, 2005. Female patient, weighting 200.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, dermatitis, erythema, facial pain, impaired healing, rash , rotator cuff syndrome, tenderness. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NORVASC, SYNTHROID, FLOVENT, ACETYLSALICYLIC ACID SRT. Patient recovered.

Bextra Side Effects Report #4752866-3
Bextra side effect was reported by a Physician from UNITED STATES on Aug 12, 2005. Female patient, weighting 200.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, dermatitis, erythema, facial pain, impaired healing, rash , rosacea . Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NORVASC, SYNTHROID, FLOVENT, ACETYLSALICYLIC ACID SRT. Patient recovered.

Bextra Side Effects Report #4873912-2
Bextra side effect was reported by a Physician from UNITED STATES on Dec 19, 2005. Female patient, weighting 178.0 lb, was diagnosed with osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: abasia, arthritis , bone disorder, condition aggravated, intervertebral disc protrusion. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient recovered.

Bextra Side Effects Report #4816763-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 19, 2005. Female patient, weighting 160.0 lb, was diagnosed with multiple sclerosis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , breast cosmetic surgery, bunion, condition aggravated, joint dislocation, treatment noncompliance, weight increased. Bextra dosage: 20 MG (10 MG, 2 IN 1 D), ORAL. During the same period patient was treated with EFFEXOR, LEXAPRO, BACLOFEN, LISINOPRIL, SKELAXIN, NEURONTIN, OXYCONTIN. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4651468-7
Bextra side effect was reported by a Consumer or non-health professional from on Apr 18, 2005. Female patient, 72 years of age, was diagnosed with meniscus lesion, blood cholesterol increased and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, condition aggravated, systemic lupus erythematosus, vasculitis . Bextra dosage: 20 MG (20 MG, 1 IN 1 D). During the same period patient was treated with EZETIMIBE, CELECOXIB, ATORVASTATIN CALCIUM, FLECAINIDE ACETATE. Patient recovered.

Bextra Side Effects Report #4617948-5
Bextra side effect was reported by a Consumer or non-health professional from on Mar 08, 2005. Female patient, 15 years of age, weighting 127.0 lb, was diagnosed with limb injury and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, condition aggravated, fall , heart rate irregular, limb injury, tachycardia, ventricular extrasystoles. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ASCORBIC ACID, ATENOLOL, MIDODRINE, FLUDROCORTISONE ACETATE. Patient recovered.

Bextra Side Effects Report #4657184-X
Bextra side effect was reported by a Consumer or non-health professional from on Apr 27, 2005. Female patient, 67 years of age, weighting 168.0 lb, was diagnosed with joint injury, dry skin and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, cerebrovascular accident, condition aggravated, dehydration, difficulty in walking, dry skin, dysstasia, fluid retention. Bextra dosage: (20 MG,) ORAL. During the same period patient was treated with CONJUGATED ESTROGENS, VITAMINS. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4708596-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on June 23, 2005. Female patient, weighting 203.0 lb, was diagnosed with inflammation and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , back pain , condition aggravated, post procedural complication, weight decreased. Bextra dosage: 20 MG (20 MG, 1 IN 1 D) ORAL. During the same period patient was treated with SYNTHROID, MORPHINE, CODEINE. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4646020-3
Bextra side effect was reported by a Physician from on Apr 13, 2005. Female patient, 86 years of age, weighting 176.4 lb, was diagnosed with ill-defined disorder, neuropathic pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac failure, condition aggravated. Bextra dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LYRICA, METHENAMINE HIPPURATE, ZOPICLONE, LANSOPRAZOLE, WARFARIN, SERETIDE MITE, PERINDOPRIL, AMITRIPTYLINE HYDROCHLORIDE. Patient died on 04/06/2005.

Bextra Side Effects Report #4650143-2
Bextra side effect was reported by a Physician from on Apr 13, 2005. Female patient, 86 years of age, weighting 176.4 lb, was diagnosed with ill-defined disorder, neuropathic pain and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac failure, condition aggravated. Bextra dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LYRICA, METHENAMINE HIPPURATE, ZOPICLONE, LANSOPRAZOLE, WARFARIN, SERETIDE MITE, PERINDOPRIL, AMITRIPTYLINE HYDROCHLORIDE. Patient died on 04/06/2005.


Bextra Side Effects Report #4649497-2
Bextra side effect was reported by a Consumer or non-health professional from on Apr 14, 2005. Male patient was diagnosed with ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac murmur, chest pain , condition aggravated, diarrhoea, dyspepsia, nausea , pneumonia , pulmonary oedema, respiratory distress. Bextra dosage: (20 MG), ORAL. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4659372-5
Bextra side effect was reported by a Consumer or non-health professional from on Apr 27, 2005. Female patient was diagnosed with ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, convulsion, gingival bleeding, haemorrhage, haemorrhagic stroke, pain in extremity, wheelchair user. Bextra dosage: 40 MG (40 MG, 1 D IN 1 D), ORAL. Patient recovered.

Bextra Side Effects Report #4760957-6
Bextra side effect was reported by a Physician from UNITED STATES on Aug 19, 2005. Male patient, weighting 254.0 lb, was diagnosed with ill-defined disorder, diabetic neuropathy, constipation , pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: back pain , blood glucose increased, blood ketone body, blood pressure increased, condition aggravated, conduction disorder, coronary artery disease , crohn's disease , diverticulum intestinal. Bextra dosage: unknown. During the same period patient was treated with OXYCONTIN, DULCOLAX, OXYCODONE, ACETYLSALICYLIC ACID SRT, AVANDIA, GLYBURIDE, LISINOPRIL, LORATADINE. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5021769-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2006. Female patient, weighting 265.0 lb, was diagnosed with ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, condition aggravated, hypertension, respiratory disorder. Bextra dosage: 10 MG (10 MG 1 IN 1D). Patient was hospitalized. Patient died on 09/20/2003.

Bextra Side Effects Report #4644974-2
Bextra side effect was reported by a Consumer or non-health professional from on Apr 08, 2005. Female patient, 56 years of age, was diagnosed with fibromyalgia and was treated with Bextra. After drug was administered, patient experienced the following side effects: abdominal pain upper, acne , allergy to animal, aphasia , blister, condition aggravated, diarrhoea, erythema, eye injury. Bextra dosage: unknown. Patient recovered.

Bextra Side Effects Report #4678414-4
Bextra side effect was reported by a Consumer or non-health professional from on May 15, 2005. Female patient, 55 years of age, weighting 148.0 lb, was diagnosed with fibromyalgia and was treated with Bextra. After drug was administered, patient experienced the following side effects: abdominal pain upper, acne , allergy to animal, aphasia , asthenia, blister, condition aggravated, contusion, diarrhoea. Bextra dosage: 20 MG (20 MG, 1 IN 1 D),. During the same period patient was treated with PREMARIN, ATIVAN. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4666383-2
Bextra side effect was reported by a Consumer or non-health professional from on May 05, 2005. Female patient, 54 years of age, weighting 188.0 lb, was diagnosed with fibromyalgia, osteoarthritis , rheumatoid arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, eyelid ptosis, retinopathy, rotator cuff repair, rotator cuff syndrome. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with GABAPENTIN, LEVOTHYROXINE, CLONAZEPAM, TRAZODONE, SINEMET, ASCORBIC ACID. Patient recovered.

Bextra Side Effects Report #5021757-5
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on May 22, 2006. Female patient, 70 years of age, was diagnosed with epicondylitis, pain , blood cholesterol increased, ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: anxiety , chest discomfort, chest pain , condition aggravated, dizziness , erythema, feeling abnormal, gastric disorder, heart rate increased. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LIPITOR, ADVIL, VITAMIN B6, VITAMIN B CAP, MAGNESIUM, CENTRUM SILVER. Patient recovered.

Bextra Side Effects Report #5150894-X
Bextra side effect was reported by a Consumer or non-health professional from CANADA on Oct 26, 2006. Female patient, 39 years of age, was diagnosed with endometriosis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: asthenia, condition aggravated, depression , mood swings, ovarian cyst , suicidal behaviour. Bextra dosage: 40 MG (40 MG, 1 IN 1 D),ORAL. Patient recovered.

Bextra Side Effects Report #5593720-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2007. Female patient, 57 years of age, weighting 123.9 lb, was diagnosed with complex regional pain syndrome , inflammation and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, depression , myocardial infarction. Bextra dosage: 20 MG (20 MG,1 IN 1 D),ORAL. Patient was hospitalized. Patient recovered.


Bextra Side Effects Report #4549604-6
Bextra side effect was reported by a Consumer or non-health professional from on Dec 23, 2004. Female patient, weighting 150.0 lb, was diagnosed with bursitis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, eye disorder, hypertension, ocular vascular disorder, urinary tract infection . Bextra dosage: unknown. During the same period patient was treated with DILTIAZEM HYDROCHLORIDE, ESOMEPRAZOLE. Patient recovered.

Bextra Side Effects Report #5270996-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 27, 2005. Female patient, 87 years of age, was diagnosed with back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: back pain , condition aggravated, epistaxis, myocardial infarction. Bextra dosage: 10 MG, ORAL. Patient recovered.

Bextra Side Effects Report #4644979-1
Bextra side effect was reported by a Consumer or non-health professional from on Apr 14, 2005. Female patient, 84 years of age, weighting 140.0 lb, was diagnosed with back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: body height decreased, cataract operation, condition aggravated, dementia , ocular vascular disorder, procedural complication. Bextra dosage: 10 MG (10 MG), ORAL. During the same period patient was treated with DONEPEZIL HYDROCHLORIDE, ATENOLOL, LEVOTHYROXINE, POTASSIUM CHLORIDE, ALENDRONATE. Patient recovered.

Bextra Side Effects Report #4590376-7
Bextra side effect was reported by a Consumer or non-health professional from on Feb 04, 2005. Male patient, 82 years of age, weighting 190.0 lb, was diagnosed with back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiac disorder, condition aggravated, dyspnoea. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ACETAMINOPHEN, POTASSIUM CHLORIDE, WARFARIN, ANTIHYPERTENSIVES. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4847022-4
Bextra side effect was reported by a Health Professional from UNITED STATES on Nov 21, 2005. Female patient, 62 years of age, weighting 205.0 lb, was diagnosed with back pain , psoriatic arthropathy, rheumatoid arthritis , spinal osteoarthritis, psoriasis and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, blister, chemical burn of skin, condition aggravated, diabetes mellitus non-insulin-dependent, disease recurrence. Bextra dosage: 20 MG (20 MG, 2 IN 1 D), ORAL. During the same period patient was treated with METHOTREXATE, ETANERCEPT, PROTOPIC, KERALYT, LOTREL. Patient recovered.

Bextra Side Effects Report #4621621-7
Bextra side effect was reported by a Consumer or non-health professional from on Mar 15, 2005. Male patient, 55 years of age, weighting 185.0 lb, was diagnosed with back pain , depression  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, depression . Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ZOLOFT, BUSPIRONE. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5594260-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2007. Male patient, 51 years of age, weighting 200.0 lb, was diagnosed with back pain , intervertebral disc protrusion, osteoarthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, hypertension, myocardial infarction, pain . Bextra dosage: 10 MG (10 MG,1 IN 1 D). Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5272068-4
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2006. Male patient, 40 years of age, weighting 270.0 lb, was diagnosed with back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: anxiety , condition aggravated, depression , hypertension, myocardial infarction. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient was hospitalized and became disabled. Patient recovered.

Bextra Side Effects Report #4651488-2
Bextra side effect was reported by a Consumer or non-health professional from on Apr 18, 2005. Male patient, 40 years of age, weighting 180.0 lb, was diagnosed with back pain , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: accident at work, acne , aggression, amnesia, anorexia, back pain , condition aggravated, convulsion, dizziness . Bextra dosage: 40 MG (20 MG, 2 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, METHADONE HYDROCHLORIDE, HYDROCODONE BITARTRATE, CLONAZEPAM, ESCITALOPRAM. Patient recovered.

Bextra Side Effects Report #4658131-7
Bextra side effect was reported by a Consumer or non-health professional from on Apr 26, 2005. Male patient, 40 years of age, weighting 180.0 lb, was diagnosed with back pain , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: accident at work, acne , aggression, amnesia, anorexia, back pain , bowel movement irregularity, condition aggravated, convulsion. Bextra dosage: 40 MG (20 MG, 2 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, METHADONE, HYDROCODONE BITARTRATE, CLONAZEPAM, ESCITALOPRAM OXALATE. Patient recovered.


Bextra Side Effects Report #4941766-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 23, 2006. Male patient, 40 years of age, weighting 180.0 lb, was diagnosed with back pain , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: accident, acne , amnesia, anger, anorexia, back pain , cheilitis, condition aggravated, constipation . Bextra dosage: 40 MG (20 MG, 2 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, METHADONE, HYDROCODONE BITARTRATE, CLONAZEPAM, ESCITALOPRAM. Patient recovered.

Bextra Side Effects Report #4698528-2
Bextra side effect was reported by a Consumer or non-health professional from on June 09, 2005. Female patient, weighting 132.0 lb, was diagnosed with back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: back pain , condition aggravated, fear, knee arthroplasty, limb injury, localised infection, rash erythematous, rash macular. Bextra dosage: 10 MG (10 MG, 1 IN 1 D) ORAL. During the same period patient was treated with CELEBREX, LOPRESSOR, VITAMIN B. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4998756-2
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 28, 2006. Female patient, weighting 178.0 lb, was diagnosed with back pain , osteoarthritis , osteoporosis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , bone disorder, condition aggravated, difficulty in walking, intervertebral disc protrusion. Bextra dosage: 20 MG (20 MG, 1 IN 1 D). Patient recovered.

Bextra Side Effects Report #4584685-5
Bextra side effect was reported by a Consumer or non-health professional from on Dec 03, 2004. Female patient, 65 years of age, was diagnosed with back disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: abnormal sensation in eye, condition aggravated, eye rolling, headache , knee arthroplasty, stomach discomfort. Bextra dosage: 20 MG (20 MG, DAILY), ORAL. During the same period patient was treated with GABAPENTIN, LORAZEPAM, VICODIN, HYDROXYZINE EMBONATE, FLUOXETINE HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5135749-9
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 30, 2006. Female patient, 87 years of age, weighting 120.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, cerebrovascular accident, chest pain , condition aggravated. Bextra dosage: unknown. Patient was hospitalized. Patient died on 02/12/2005.

Bextra Side Effects Report #5085655-3
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2006. Male patient, 85 years of age, weighting 161.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: apnoea, bradycardia, cerebrovascular accident, chronic obstructive pulmonary disease, condition aggravated, cough, dyspnoea, facial palsy. Bextra dosage: 10 MG (1 IN 1 D). Patient was hospitalized. Patient died on 10/10/2004.

Bextra Side Effects Report #5122201-X
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 01, 2006. Male patient, 85 years of age, weighting 161.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: apnoea, bradycardia, bronchitis , cardiac arrest , cerebrovascular accident, chronic obstructive pulmonary disease, condition aggravated, loss of consciousness. Bextra dosage: 10 MG (1 IN 1 D). Patient was hospitalized. Patient died on 10/10/2004.

Bextra Side Effects Report #5172285-8
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 23, 2006. Male patient, 82 years of age, weighting 180.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: cardiovascular disorder, condition aggravated, coronary artery disease , injury, myocardial infarction. Bextra dosage: 10 MG (10 MG, 1 IN 1 D). Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5046284-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on June 15, 2006. Female patient, 80 years of age, was diagnosed with arthritis , neuralgia and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , condition aggravated, faeces discoloured, gastric haemorrhage, myocardial infarction, neuralgia, pollakiuria, post procedural complication. Bextra dosage: unknown. During the same period patient was treated with LYRICA, MICARDIS, PLAVIX, HYDROCHLOROTHIAZIDE, ZOCOR. Patient was hospitalized and became disabled. Patient recovered.

Bextra Side Effects Report #5594259-5
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 12, 2007. Male patient, 79 years of age, weighting 195.1 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: anxiety , cardiac failure, condition aggravated, headache , hypertension, myocardial infarction. Bextra dosage: 10 MG (10 MG,1 IN 1 D). Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4661977-2
Bextra side effect was reported by a Consumer or non-health professional from on Apr 14, 2005. Female patient, 76 years of age, weighting 171.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: blood pressure fluctuation, cerebrovascular accident, condition aggravated, difficulty in walking, false positive laboratory result, loss of consciousness, rash pruritic, scratch, skin haemorrhage. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with OMEPRAZOLE, THYROID, ASCORBIC ACID, CENTRUM SILVER, CALCIUM CARBONATE, ASPIRIN, DIPYRIDAMOLE. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4741446-1
Bextra side effect was reported by a Physician from UNITED STATES on July 28, 2005. Female patient, 75 years of age, weighting 132.0 lb, was diagnosed with arthritis , back pain  and was treated with Bextra. After drug was administered, patient experienced the following side effects: back pain , condition aggravated, infection , rash , scar , stomach discomfort. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, LOPRESSOR, VITAMIN B12. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4998764-1
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 27, 2006. Female patient, 75 years of age, weighting 230.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: atrioventricular block, condition aggravated, heart rate irregular, myocardial infarction. Bextra dosage: unknown. Patient was hospitalized. Patient died on 10/16/2004.

Bextra Side Effects Report #5014487-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on May 12, 2006. Female patient, 75 years of age, weighting 230.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: atrioventricular block, blood pressure increased, cardio-respiratory arrest, colonic polyp , condition aggravated, gastric ulcer, gastritis, gastrointestinal haemorrhage, heart rate irregular. Bextra dosage: 10 MG (10 MG, 1 IN 1 D). Patient was hospitalized. Patient died on 10/16/2004.

Bextra Side Effects Report #5594248-0
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2007. Female patient, 74 years of age, weighting 179.9 lb, was diagnosed with arthritis , pain management and was treated with Bextra. After drug was administered, patient experienced the following side effects: condition aggravated, hypertension, myocardial infarction. Bextra dosage: 10 MG. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #4684535-2
Bextra side effect was reported by a Consumer or non-health professional from on May 23, 2005. Female patient, 74 years of age, weighting 190.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: acarodermatitis, condition aggravated, dyspnoea, feeling abnormal, nasal sinus drainage, nasopharyngitis, rash pruritic, scar , skin infection. Bextra dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TOPROL, PRINIVIL, PROZAC, ZOCOR, FOSAMAX, SYNTHROID, ASPIRIN. Patient was hospitalized. Patient recovered.

Bextra Side Effects Report #5146349-9
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2006. Female patient, 70 years of age, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: actinic keratosis, asthma , blood pressure increased, bronchitis acute, bursitis , condition aggravated, fibromyalgia, hypersomnia, influenza. Bextra dosage: 10 MG. During the same period patient was treated with CELEBREX, VIOXX. Patient recovered.

Bextra Side Effects Report #4642084-1
Bextra side effect was reported by a Consumer or non-health professional from on Apr 07, 2005. Female patient, 70 years of age, weighting 124.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthritis , blood pressure fluctuation, body height decreased, cataract , cerebrospinal fluid leakage, condition aggravated, cough, dry skin, gastric disorder. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with FUROSEMIDE, CONJUGATED ESTROGENS. Patient recovered.

Bextra Side Effects Report #4655586-9
Bextra side effect was reported by a Consumer or non-health professional from on Apr 22, 2005. Female patient, 70 years of age, weighting 124.0 lb, was diagnosed with arthritis , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, arthritis , arthropathy, blood pressure fluctuation, body height decreased, cataract , cerebrospinal fluid leakage, condition aggravated, cough. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, FUROSEMIDE, CONJUGATED ESTROGENS. Patient recovered.

Bextra Side Effects Report #4657242-X
Bextra side effect was reported by a Physician from on Apr 27, 2005. Female patient, 70 years of age, weighting 124.0 lb, was diagnosed with arthritis , ill-defined disorder and was treated with Bextra. After drug was administered, patient experienced the following side effects: arthralgia, arthritis , arthropathy, body height decreased, cataract , cerebrospinal fluid leakage, condition aggravated, feeling abnormal, gastric disorder. Bextra dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CELEBREX, FUROSEMIDE, CONJUGATED ESTROGENS. Patient recovered.

Bextra Side Effects Report #4873923-7
Bextra side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 21, 2005. Female patient, 68 years of age, weighting 170.0 lb, was diagnosed with arthritis  and was treated with Bextra. After drug was administered, patient experienced the following side effects: chronic obstructive pulmonary disease, condition aggravated, crying, dyspnoea, emphysema, fatigue, memory impairment, nasopharyngitis, staphylococcal infection . Bextra dosage: unknown. During the same period patient was treated with NORVASC, ADVAIR DISKUS, COMBIVENT, DUONEB, SPIRIVA, KLONOPIN. Patient was hospitalized. Patient recovered.