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Oxaprozin adverse events reported to FDA.

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Summary

FDA Adverse Reports: 26. View All

Oxaprozin FDA safety alerts: No

Reported hospitalizations: 12

Oxaprozin Dosage, Warnings, Usage.

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Often additional risks of using a medication, such as Oxaprozin, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Oxaprozin users, Learn more about unwanted side effects & find ways to reduce them. Browse Oxaprozin Adverse Reports reported to FDA and participate in Oxaprozin discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Oxaprozin. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Oxaprozin Adverse Effect Reports (FDA)

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6477596-1 | Pain, Product Substitution Issue
on Dec 03, 2009 Female patient from UNITED STATES , weighting 180.0 lb, was diagnosed with arthralgia and was treated with Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: pain (What is pain?), product substitution issue. Oxaprozin dosage: 600mg Bid Po.

6391084-2 | Gastric Haemorrhage, Gastric Ulcer, Gastroenteritis, Gastrointestinal Haemorrhage, Haemoglobin Decreased
Patient was taking Oxaprozin (View Usage). Patient had the following side effects: gastric haemorrhage, gastric ulcer, gastroenteritis (What is gastroenteritis?), gastrointestinal haemorrhage, haemoglobin decreased on Oct 06, 2009 from UNITED STATES Additional patient health information: Male patient , 53 years of age, weighting 203.9 lb, was diagnosed with pain (What is pain?) and. Oxaprozin dosage: 600 Mg Bid Po. During the same period patient was treated with NAPROXEN (500 Mg Bid Po) (View Naproxen Review and Naproxen Label ). Patient was hospitalized.

6391041-6 | Withdrawal Syndrome
Adverse event was reported on Oct 06, 2009 by a Male patient taking Oxaprozin (View Usage) (Dosage: ) was diagnosed with affective disorder and. Location: UNITED STATES , 61 years of age, weighting 175.0 lb, After Oxaprozin was administered, patient had the following side effects: withdrawal syndrome. During the same period patient was treated with OXCARBAZEPINE (View Oxcarbazepine Review and Oxcarbazepine Label ).

6193335-6 | Gastrointestinal Haemorrhage
on May 14, 2009 Female patient from UNITED STATES , 77 years of age, was diagnosed with arthritis (What is arthritis?) and was treated with Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal haemorrhage. Oxaprozin dosage: 1200mg Daily Po. Patient was hospitalized.


6085921-9 | Dysphasia, Dysphemia, Sensation Of Heaviness, Tremor
on Feb 17, 2009 Female patient from UNITED STATES , weighting 190.0 lb, was diagnosed with pain in extremity and was treated with Oxaprozin (View Usage). Patient had the following side effects: dysphasia, dysphemia, sensation of heaviness, tremor. Oxaprozin dosage: 1 Tablet Twice Daily As Nee Po. Patient was hospitalized.

6051708-6 | Arthralgia, Joint Stiffness
Patient was taking Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: arthralgia, joint stiffness on Jan 21, 2009 from UNITED STATES Additional patient health information: Female patient , 82 years of age, weighting 125.0 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Oxaprozin dosage: 1200 Mg Daily Po.

5910408-0 | Hypersensitivity
Adverse event was reported on Oct 06, 2008 by a Male patient taking Oxaprozin (View Usage) (Dosage: 2 Tablets Once Daily Po Taken One Time) was diagnosed with exostosis and. Location: UNITED STATES , 59 years of age, weighting 250.0 lb, Patient experienced the following unwanted or unexpected effects: hypersensitivity. Patient was hospitalized.

5892262-9 | Gastrointestinal Haemorrhage, Petit Mal Epilepsy
on Sep 08, 2008 Male patient from UNITED STATES , 82 years of age, was treated with Oxaprozin (View Usage). Patient had the following side effects: gastrointestinal haemorrhage, petit mal epilepsy. Oxaprozin dosage: 18 Pills,. During the same period patient was treated with OXCARBAZAPINE 600 MG (View Oxcarbazapine 600 Mg Review and Oxcarbazapine 600 Mg Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), LOW DOSAGE ASPIRIN (View Low Dosage Aspirin Review and Low Dosage Aspirin Label ), GLUCOPHAGE XR (View Glucophage Xr Review and Glucophage Xr Label ), CRESTOR (View Crestor Review and Crestor Label ), SPIRIVA (View Spiriva Review and Spiriva Label ). Patient was hospitalized.

5885299-7 | Blood Urine Present, Eye Swelling, Gastrointestinal Disorder, Haematochezia, Pharyngeal Oedema, Renal Disorder, Urticaria
on Sep 15, 2008 Male patient from UNITED STATES , 32 years of age, weighting 143.0 lb, was diagnosed with back pain (What is back pain?), muscle spasms and was treated with Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: blood urine present, eye swelling, gastrointestinal disorder, haematochezia, pharyngeal oedema, renal disorder, urticaria. Oxaprozin dosage: One Tablet Twice A Day Po. Patient was hospitalized.

5868786-7 | Grand Mal Convulsion
Patient was taking Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: grand mal convulsion on Aug 19, 2008 from UNITED STATES Additional patient health information: Female patient , 27 years of age, . Oxaprozin dosage: . During the same period patient was treated with OXCARBAZEPINE (View Oxcarbazepine Review and Oxcarbazepine Label ).

5852278-5 | Grand Mal Convulsion
Adverse event was reported on Aug 20, 2008 by a Female patient taking Oxaprozin (View Usage) (Dosage: Tablet) . Location: UNITED STATES , 27 years of age, Patient had the following side effects: grand mal convulsion. During the same period patient was treated with OXCARBAZEPINE (Tablet) (View Oxcarbazepine Review and Oxcarbazepine Label ).

5840488-2 | Discomfort, Pruritus
on Aug 07, 2008 Male patient from UNITED STATES , 78 years of age, weighting 162.0 lb, was diagnosed with myalgia and was treated with Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: discomfort, pruritus. Oxaprozin dosage: 600 Mg Twice A Day Po.

5759432-1 | Blood Pressure Increased, Flushing, Hypersensitivity, Oedema Mouth, Pruritus, Swelling Face
on Jun 04, 2008 Male patient from UNITED STATES , 44 years of age, weighting 270.0 lb, was diagnosed with plantar fasciitis and was treated with Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, flushing, hypersensitivity, oedema mouth, pruritus, swelling face. Oxaprozin dosage: 1-600 Mg Tablets By Mouth.

5736988-6 | Anaemia, Chest Pain, Dizziness, Duodenal Ulcer Haemorrhage, Hypotension, Melaena, Refusal Of Treatment By Relative
Patient was taking Oxaprozin (View Usage). Patient had the following side effects: anaemia, chest pain (What is chest pain?), dizziness (What is dizziness?), duodenal ulcer haemorrhage, hypotension, melaena, refusal of treatment by relative on May 13, 2008 from UNITED STATES Additional patient health information: Female patient , 92 years of age, was diagnosed with arthritis (What is arthritis?) and. Oxaprozin dosage: 600mg Daily Po. Patient was hospitalized.

5728317-9 | Contusion, Haemorrhage
Adverse event was reported on May 02, 2008 by a Female patient taking Oxaprozin (View Usage) (Dosage: 1 Tablet Every 12 Hours Po) was diagnosed with joint swelling and. Location: UNITED STATES , 45 years of age, weighting 150.0 lb, After Oxaprozin was administered, patient had the following side effects: contusion, haemorrhage.

5466653-4 | Biopsy Liver Abnormal, Hepatic Necrosis, Hepatitis, Hepatomegaly, Liver Injury, Night Sweats, Rash Maculo-papular, Splenomegaly, Tenderness
on Sep 24, 2007 Female patient from UNITED STATES , 45 years of age, was treated with Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: biopsy liver abnormal, hepatic necrosis, hepatitis (What is hepatitis?), hepatomegaly, liver injury, night sweats, rash maculo-papular, splenomegaly, tenderness. Oxaprozin dosage: 600 Mg Tabs. During the same period patient was treated with YASMIN (View Yasmin Review and Yasmin Label ), SEASONALE (ETHINYL ESTRADIOL LEVONORGESTREL) (View Seasonale (ethinyl Estradiol -levonorgestrel) Review and Seasonale (ethinyl Estradiol -levonorgestrel) Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ), FLOVENT (View Flovent Review and Flovent Label ), SINGULAIR (View Singulair Review and Singulair Label ), OMEGA 6 FISH OIL (View Omega-6 Fish Oil Review and Omega-6 Fish Oil Label ), CALCIUM (View Calcium Review and Calcium Label ), CHROMIUM (View Chromium Review and Chromium Label ).

5342070-2 | Rash, Scar, Toxic Epidermal Necrolysis
on Mar 24, 2005 Female patient from UNITED STATES , 51 years of age, was diagnosed with pyrexia and was treated with Oxaprozin (View Usage). Patient had the following side effects: rash (What is rash?), scar (What is scar?), toxic epidermal necrolysis. Oxaprozin dosage: .

5122913-8 | Diarrhoea
Patient was taking Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: diarrhoea on Oct 04, 2006 from UNITED STATES Additional patient health information: Male patient , 57 years of age, weighting 218.3 lb, was diagnosed with inflammation, pain (What is pain?) and. Oxaprozin dosage: 1200 Mg Po Qd.

5013473-0 | Angioneurotic Oedema, Urticaria
Adverse event was reported on May 25, 2006 by a Female patient taking Oxaprozin (View Usage) (Dosage: 600 Mg Daily Po (duration: A Few Days)) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , 64 years of age, Patient experienced the following unwanted or unexpected effects: angioneurotic oedema, urticaria.

4951605-0 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Albumin Decreased, Blood Alkaline Phosphatase Increased, Blood Glucose Increased, Blood Potassium Increased, Cardiac Murmur, Cough, Dialysis
on Mar 03, 2006 Female patient from UNITED STATES , 39 years of age, weighting 176.0 lb, was diagnosed with back pain (What is back pain?), hypertension, adnexa uteri pain and was treated with Oxaprozin (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood glucose increased, blood potassium increased, cardiac murmur, cough, dialysis (What is dialysis?). Oxaprozin dosage: 600 Mg Po. During the same period patient was treated with LISINOPRIL AND HYDROCHLOROTHIAZIDE (1 Tab Daily Po) (View Lisinopril And Hydrochlorothiazide Review and Lisinopril And Hydrochlorothiazide Label ), CELEBREX (200 Mg Bid Po) (View Celebrex Review and Celebrex Label ). Patient was hospitalized.

4865707-0 | Dialysis, Influenza Like Illness, Renal Failure, Renal Injury, Vomiting
on May 17, 2004 Female patient from UNITED STATES , 39 years of age, was diagnosed with back pain (What is back pain?), hypertension and was treated with Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: dialysis (What is dialysis?), influenza like illness, renal failure, renal injury, vomiting. Oxaprozin dosage: 600 Mg Po. During the same period patient was treated with LISINOPRIL/HCTZ EON LABS (Po) (View Lisinopril/hctz Eon Labs Review and Lisinopril/hctz Eon Labs Label ). Patient was hospitalized.

4790445-2 | Blood Glucose Increased, Blood Pressure Decreased, Oedema Peripheral, Pulmonary Embolism, Skin Ulcer, Tachycardia
Patient was taking Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: blood glucose increased, blood pressure decreased, oedema peripheral, pulmonary embolism (What is pulmonary embolism?), skin ulcer, tachycardia on Sep 22, 2005 from UNITED STATES Additional patient health information: Female patient , 54 years of age, weighting 402.1 lb, . Oxaprozin dosage: . During the same period patient was treated with FUROSEMIDE (View Furosemide Review and Furosemide Label ), SPIRONOLACTONE (View Spironolactone Review and Spironolactone Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), GLYCERYL TRINITRATE (View Glyceryl Trinitrate Review and Glyceryl Trinitrate Label ). Patient was hospitalized.

4767060-X | Cellulitis, Gastric Ulcer, Haematocrit Decreased, Haemoglobin Decreased, Melaena
Adverse event was reported on Sep 08, 2005 by a Female patient taking Oxaprozin (View Usage) (Dosage: 600 Mg Bid [chronic]) was diagnosed with pain (What is pain?), rheumatoid arthritis (What is rheumatoid arthritis?) and. Location: UNITED STATES , 89 years of age, weighting 156.5 lb, Patient had the following side effects: cellulitis (What is cellulitis?), gastric ulcer, haematocrit decreased, haemoglobin decreased, melaena. During the same period patient was treated with PREDNISONE (2 Mg Qd [chronic]) (View Prednisone Review and Prednisone Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), DYAZIDE (View Dyazide Review and Dyazide Label ), AVAPRO (View Avapro Review and Avapro Label ), CALCIUM CARB (View Calcium Carb Review and Calcium Carb Label ), CARDIZEM (View Cardizem Review and Cardizem Label ). Patient was hospitalized.

4624431-X | Febrile Neutropenia
on Mar 30, 2005 Female patient from , weighting 219.0 lb, was diagnosed with fibromyalgia and was treated with Oxaprozin (View Usage). After Oxaprozin was administered, patient had the following side effects: febrile neutropenia. Oxaprozin dosage: 1200mg Daily Oral. Patient was hospitalized.

4586916-4 | Dizziness, Feeling Abnormal, Gait Disturbance, Irritability, Urticaria
on Feb 15, 2005 Female patient from , 54 years of age, weighting 160.0 lb, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Oxaprozin (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), feeling abnormal, gait disturbance, irritability, urticaria. Oxaprozin dosage: 600mg 2 Times A Day Oral.

4552643-2 | Abnormal Dreams, Fatigue, Hypersomnia
Patient was taking Oxaprozin (View Usage). Patient had the following side effects: abnormal dreams, fatigue, hypersomnia on Jan 12, 2005 from Additional patient health information: Female patient , 63 years of age, . Oxaprozin dosage: .


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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Oxaprozin risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Oxaprozin quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Oxaprozin use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Oxaprozin Reactions
Abnormal Dreams
Alanine Aminotransferase Increased
Anaemia
Angioneurotic Oedema
Arthralgia
Aspartate Aminotransferase Increased
Biopsy Liver Abnormal
Blood Albumin Decreased
Blood Alkaline Phosphatase Increased
Blood Glucose Increased
Blood Potassium Increased
Blood Pressure Decreased
Blood Pressure Increased
Blood Urine Present
Cardiac Murmur
CellulitisWhat is Cellulitis?
Chest PainWhat is Chest pain?
Contusion
Cough
DialysisWhat is Dialysis?
Diarrhoea
DizzinessWhat is Dizziness?
Gastric Ulcer
Gastrointestinal Haemorrhage
Grand Mal Convulsion
Haemoglobin Decreased
Hypersensitivity
Melaena
Pruritus
Urticaria
Oxaprozin Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Oxaprozin adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!