DAYPRO Side Effects

6804172-0 | Abdominal Pain Upper
on Jan 22, 2007 Male patient from UNITED STATES , weighting 185.0 lb, was treated with Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper. Daypro dosage: .

6788790-4 | Dysarthria
Patient was taking Daypro (View Usage). Patient had the following side effects: dysarthria on May 22, 2008 from UNITED STATES Additional patient health information: Female patient , 40 years of age, weighting 110.2 lb, . Daypro dosage: .

6788564-4 | Renal Failure
Adverse event was reported on May 06, 2008 by a Female patient taking Daypro (View Usage) (Dosage: ) was diagnosed with migraine (What is migraine?) and. Location: UNITED STATES , weighting 310.9 lb, After Daypro was administered, patient had the following side effects: renal failure. During the same period patient was treated with NAPROXEN (View Naproxen Review and Naproxen Label ), LOTREL (5/20 Daily) (View Lotrel Review and Lotrel Label ), NORTRIPTYLINE (At Bedtime) (View Nortriptyline Review and Nortriptyline Label ), VOSOL HC (View Vosol Hc Review and Vosol Hc Label ), MUCINEX (View Mucinex Review and Mucinex Label ), FIORICET W/ CODEINE (View Fioricet W/ Codeine Review and Fioricet W/ Codeine Label ), KUTRASE (Daily) (View Kutrase Review and Kutrase Label ).

6611612-9 | Myocardial Infarction
on Dec 15, 2009 Male patient from UNITED STATES , 44 years of age, weighting 210.1 lb, was diagnosed with headache (What is headache?) and was treated with Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Daypro dosage: .


6611607-5 | Dyspnoea, Hypersensitivity, Throat Tightness
on Apr 16, 2009 Female patient from UNITED STATES , weighting 280.0 lb, was diagnosed with back pain (What is back pain?) and was treated with Daypro (View Usage). Patient had the following side effects: dyspnoea, hypersensitivity, throat tightness. Daypro dosage: 600 Mg.

6419093-5 | Anaphylactic Reaction, Erythema, Pharyngeal Oedema, Pruritus
Patient was taking Daypro (View Usage). After Daypro was administered, patient had the following side effects: anaphylactic reaction, erythema, pharyngeal oedema, pruritus on Oct 28, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 173.0 lb, was diagnosed with arthralgia and. Daypro dosage: 1200 Mg Daily. During the same period patient was treated with LIDODERM PATCH FOR 12 HOURS NIGHTLY (View Lidoderm Patch For 12 Hours Nightly Review and Lidoderm Patch For 12 Hours Nightly Label ), AVAPRO (View Avapro Review and Avapro Label ). Patient was hospitalized.

6045190-2 | Rectal Haemorrhage
Adverse event was reported on Jan 16, 2009 by a Female patient taking Daypro (View Usage) (Dosage: 600 Mg Tablet Mg Bid Oral) . Location: UNITED STATES , weighting 185.4 lb, Patient experienced the following unwanted or unexpected effects: rectal haemorrhage. During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), DOXYCYCLINE HYCLATE (View Doxycycline Hyclate Review and Doxycycline Hyclate Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), NEXIUM (View Nexium Review and Nexium Label ), NORVASC (View Norvasc Review and Norvasc Label ), PLAQUENIL (HYROXYCHLOROQUINE) (View Plaquenil (hyroxychloroquine) Review and Plaquenil (hyroxychloroquine) Label ), SIMAVASTATIN (View Simavastatin Review and Simavastatin Label ), TRICOR (FENOFIBRATE (TRICOR)) (View Tricor (fenofibrate (tricor)) Review and Tricor (fenofibrate (tricor)) Label ). Patient was hospitalized.

5664387-4 | Hepatitis
on Mar 11, 2008 Female patient from UNITED STATES , 66 years of age, was treated with Daypro (View Usage). Patient had the following side effects: hepatitis (What is hepatitis?). Daypro dosage: . Patient was hospitalized.

5320311-5 | Colitis Ulcerative, Condition Aggravated, Haematochezia, Irritable Bowel Syndrome
on Mar 20, 2006 Female patient from UNITED STATES , 80 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?), urinary incontinence (What is urinary incontinence?) and was treated with Daypro (View Usage). After Daypro was administered, patient had the following side effects: colitis ulcerative, condition aggravated, haematochezia, irritable bowel syndrome (What is irritable bowel syndrome?). Daypro dosage: 1200 Mg (600 Mg,2 In 1 D),oral. During the same period patient was treated with OXYBUTYNIN CHLORIDE ((3.9 Mg,1 In 2 Wk), Transdermal) (View Oxybutynin Chloride Review and Oxybutynin Chloride Label ), IBUPROFEN (Oral) (View Ibuprofen Review and Ibuprofen Label ), DITROPAN XL (View Ditropan Xl Review and Ditropan Xl Label ), ROBINUL (GLYCOPYRRONIUM BROMIDE) (View Robinul (glycopyrronium Bromide) Review and Robinul (glycopyrronium Bromide) Label ), PROCHLORPERAZINE MALEATE (View Prochlorperazine Maleate Review and Prochlorperazine Maleate Label ). Patient was hospitalized.

4974849-0 | Renal Failure
Patient was taking Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: renal failure on Feb 18, 2005 from UNITED STATES Additional patient health information: Male patient , 55 years of age, was diagnosed with arthritis (What is arthritis?), cardiac failure congestive, hypertension and. Daypro dosage: 600 Mg (600 Mg, 1 In 1 D), Oral. During the same period patient was treated with OLMESARTAN MEDOXOMIL (OLMESARTAN MEDOXOMIL) ((daily), Oral) (View Olmesartan Medoxomil (olmesartan Medoxomil) Review and Olmesartan Medoxomil (olmesartan Medoxomil) Label ), BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE (View Bisoprolol Fumarate And Hydrochlorothiazide Review and Bisoprolol Fumarate And Hydrochlorothiazide Label ), AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ), FLUVASTATIN SODIUM (FLUVASTATIN SODIUM) (View Fluvastatin Sodium (fluvastatin Sodium) Review and Fluvastatin Sodium (fluvastatin Sodium) Label ), PIOGLITAZONE HCL (View Pioglitazone Hcl Review and Pioglitazone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

4970907-5 | Angioneurotic Oedema, Urticaria
Adverse event was reported on Apr 11, 2006 by a Male patient taking Daypro (View Usage) (Dosage: ) . Location: UNITED STATES , 57 years of age, weighting 252.4 lb, Patient had the following side effects: angioneurotic oedema, urticaria.

4882499-X | Gastric Ulcer, Gastritis, Gastritis Erosive, Gastrooesophageal Reflux Disease, Vertigo
on Jan 03, 2006 Female patient from UNITED STATES , 80 years of age, weighting 269.9 lb, was diagnosed with ill-defined disorder, thrombosis prophylaxis and was treated with Daypro (View Usage). After Daypro was administered, patient had the following side effects: gastric ulcer, gastritis, gastritis erosive, gastrooesophageal reflux disease, vertigo. Daypro dosage: Oral. During the same period patient was treated with ASPIRIN (1 In 1 D, Oral) (View Aspirin Review and Aspirin Label ), VALSARTAN (View Valsartan Review and Valsartan Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label ).

4845280-3 | Arthralgia, Blood Glucose Increased, Calcinosis, Dizziness, Ligament Disorder, Malaise, Nasal Congestion, Seasonal Allergy, Stomach Discomfort
on Nov 15, 2005 Female patient from UNITED STATES , 54 years of age, weighting 225.0 lb, was diagnosed with joint injury and was treated with Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, blood glucose increased, calcinosis, dizziness (What is dizziness?), ligament disorder, malaise, nasal congestion, seasonal allergy, stomach discomfort. Daypro dosage: . During the same period patient was treated with CELEBREX (200 Mg (200 Mg, 1 In 1d)) (View Celebrex Review and Celebrex Label ), BEXTRA (10 Mg (10 Mg, 1in 1d)) (View Bextra Review and Bextra Label ), GLUCOSAMINE (GLUCOSAMINE) (View Glucosamine (glucosamine) Review and Glucosamine (glucosamine) Label ). Patient was hospitalized.

4809179-0 | Gastrointestinal Haemorrhage, Gastrointestinal Ulcer
Patient was taking Daypro (View Usage). Patient had the following side effects: gastrointestinal haemorrhage, gastrointestinal ulcer on Oct 21, 2005 from UNITED STATES Additional patient health information: Female patient , 91 years of age, weighting 123.5 lb, . Daypro dosage: Po. Patient was hospitalized.

4744421-6 | Chest Pain
Adverse event was reported on Aug 11, 2005 by a Male patient taking Daypro (View Usage) (Dosage: One Po Bid) was diagnosed with angina pectoris and. Location: UNITED STATES , 25 years of age, weighting 164.0 lb, After Daypro was administered, patient had the following side effects: chest pain (What is chest pain?).

4701074-0 | Chest Pain, Dyspnoea, Knee Arthroplasty, Pulmonary Embolism
on Jun 15, 2005 Female patient from , 75 years of age, weighting 174.0 lb, was diagnosed with arthritis (What is arthritis?) and was treated with Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dyspnoea, knee arthroplasty, pulmonary embolism (What is pulmonary embolism?). Daypro dosage: . During the same period patient was treated with CELEBREX (200 Mg (200 Mg 1 In 1 D) Oral) (View Celebrex Review and Celebrex Label ), BEXTRA (10 Mg (10 Mg 1 In 1 D) Oral) (View Bextra Review and Bextra Label ), VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized.

4690206-9 | Chest Pain, Knee Arthroplasty, Pulmonary Embolism
on Jun 01, 2005 Male patient from , 75 years of age, weighting 174.0 lb, was diagnosed with arthritis (What is arthritis?) and was treated with Daypro (View Usage). Patient had the following side effects: chest pain (What is chest pain?), knee arthroplasty, pulmonary embolism (What is pulmonary embolism?). Daypro dosage: . During the same period patient was treated with CELEBREX (200 Mg (200 Mg, 1 In 1 D), Oral) (View Celebrex Review and Celebrex Label ), BEXTRA (10 Mg (10 Mg, 1 In 1 D), Oral) (View Bextra Review and Bextra Label ), VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized.

4686212-0 | Endoscopy, Nerve Injury, Pain, Stomach Discomfort, Surgery
Patient was taking Daypro (View Usage). After Daypro was administered, patient had the following side effects: endoscopy (What is endoscopy?), nerve injury, pain (What is pain?), stomach discomfort, surgery (What is surgery?) on May 24, 2005 from Additional patient health information: Male patient , 40 years of age, weighting 200.0 lb, was diagnosed with nerve injury and. Daypro dosage: 1600 Mg (1 In 1 D) Oral. During the same period patient was treated with BEXTRA (20 Mg (10 Mg, 2 In 1 D) Oral) (View Bextra Review and Bextra Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), ELAVIL (View Elavil Review and Elavil Label ), DESIPRAMIDE HCL (View Desipramide Hcl Review and Desipramide Hcl Label ), DEPAKOTE (View Depakote Review and Depakote Label ), TEGRETOL (View Tegretol Review and Tegretol Label ), LAMICTAL (View Lamictal Review and Lamictal Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ).

4681111-2 | Depression, Food Intolerance, Hypertension, Pain, Small Intestinal Obstruction, Unevaluable Event
Adverse event was reported on May 19, 2005 by a Female patient taking Daypro (View Usage) (Dosage: ) was diagnosed with osteitis and. Location: , 42 years of age, Patient experienced the following unwanted or unexpected effects: depression (What is depression?), food intolerance, hypertension, pain (What is pain?), small intestinal obstruction, unevaluable event. During the same period patient was treated with MOTRIN (800 Mg Tid, Oral) (View Motrin Review and Motrin Label ), INDOMETHACIN (View Indomethacin Review and Indomethacin Label ), ANALGESICS (ANALGESICS) (View Analgesics (analgesics) Review and Analgesics (analgesics) Label ). Patient was hospitalized.

4672919-8 | Condition Aggravated, Hypertonic Bladder, Tremor
on May 09, 2005 Female patient from , 69 years of age, weighting 155.0 lb, was diagnosed with ill-defined disorder and was treated with Daypro (View Usage). Patient had the following side effects: condition aggravated, hypertonic bladder, tremor. Daypro dosage: . During the same period patient was treated with DOXYCYCLINE (View Doxycycline Review and Doxycycline Label ).

4663715-6 | Angiopathy, Barrett's Oesophagus, Chest Pain, Gastrooesophageal Reflux Disease, Haemorrhage, Hiatus Hernia, Oesophageal Ulcer, Pancreatitis, Weight Decreased
on Dec 22, 2004 Female patient from , 56 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Daypro (View Usage). After Daypro was administered, patient had the following side effects: angiopathy, barrett's oesophagus, chest pain (What is chest pain?), gastrooesophageal reflux disease, haemorrhage, hiatus hernia, oesophageal ulcer, pancreatitis, weight decreased. Daypro dosage: (2 In 1 D), Oral.

4654191-8 | Chest Pain, Dyspnoea, Knee Arthroplasty, Pulmonary Embolism
Patient was taking Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: chest pain (What is chest pain?), dyspnoea, knee arthroplasty, pulmonary embolism (What is pulmonary embolism?) on Apr 21, 2005 from Additional patient health information: Male patient , 75 years of age, weighting 174.0 lb, was diagnosed with arthritis (What is arthritis?) and. Daypro dosage: . During the same period patient was treated with CELEBREX (200 Mg (200 Mg, 1 In 1 D) Oral) (View Celebrex Review and Celebrex Label ), BEXTRA (10 Mg (10 Mg, 1 In 1 D) Oral) (View Bextra Review and Bextra Label ), ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ). Patient was hospitalized.

4648285-0 | Knee Arthroplasty, Pulmonary Embolism
Adverse event was reported on Apr 13, 2005 by a Male patient taking Daypro (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?) and. Location: , 75 years of age, weighting 174.0 lb, Patient had the following side effects: knee arthroplasty, pulmonary embolism (What is pulmonary embolism?). During the same period patient was treated with CELEBREX (200 Mg (200 Mg, 1 In 1 D), Oral) (View Celebrex Review and Celebrex Label ), BEXTRA (10 Mg (10 Mg, 1 In 1 D), Oral) (View Bextra Review and Bextra Label ), ROFECOXIB (View Rofecoxib Review and Rofecoxib Label ). Patient was hospitalized.

4647254-4 | Nerve Injury, Pain, Procedural Complication
on Apr 12, 2005 Male patient from , weighting 200.0 lb, was diagnosed with nerve injury and was treated with Daypro (View Usage). After Daypro was administered, patient had the following side effects: nerve injury, pain (What is pain?), procedural complication. Daypro dosage: 1600 Mg (1 In 1d ) Oral. During the same period patient was treated with BEXTRA (10 Mg (10 Mg 2 In 1 D) Oral) (View Bextra Review and Bextra Label ), METHADONE HCL (View Methadone Hcl Review and Methadone Hcl Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), DESIPRAMINE HCL (View Desipramine Hcl Review and Desipramine Hcl Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ), CARBAMAZEPINE (View Carbamazepine Review and Carbamazepine Label ), LAMOTRIGINE (View Lamotrigine Review and Lamotrigine Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ).

4602218-1 | Glomerulonephritis Membranous, Urinary Tract Infection
on Oct 30, 2003 Female patient from , 46 years of age, weighting 140.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Daypro (View Usage). Patient experienced the following unwanted or unexpected effects: glomerulonephritis membranous, urinary tract infection (What is urinary tract infection?). Daypro dosage: . During the same period patient was treated with ETANERCEPT (ETANERCEPT) (25 Mg, Biweekly, Subcutaneous) (View Etanercept (etanercept) Review and Etanercept (etanercept) Label ), CITALOPRAM HYDROBROMIDE (View Citalopram Hydrobromide Review and Citalopram Hydrobromide Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), FLUTICASONE PROPIONATE (View Fluticasone Propionate Review and Fluticasone Propionate Label ), ALBUTEROL SULFATE (View Albuterol Sulfate Review and Albuterol Sulfate Label ), VITAMINS (View Vitamins Review and Vitamins Label ). Patient was hospitalized.

4562047-4 | Aortic Disorder, Fall, Haemorrhage, Hepatocellular Damage, Rectal Haemorrhage
Patient was taking Daypro (View Usage). Patient had the following side effects: aortic disorder, fall (What is fall?), haemorrhage, hepatocellular damage, rectal haemorrhage on Feb 10, 2004 from Additional patient health information: Male patient , 80 years of age, weighting 170.0 lb, was diagnosed with arthritis (What is arthritis?), ischaemic stroke and. Daypro dosage: Qd, Oral. During the same period patient was treated with PLAVIX (75 Mg, Qd, Oral) (View Plavix Review and Plavix Label ), ASPIRIN (325 Mg, Qd, Oral) (View Aspirin Review and Aspirin Label ). Patient was hospitalized.