Arcoxia Side Effects

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Arcoxia adverse events reported to FDA.

Have You Experienced unusual Arcoxia symptoms? PatientsVille.com collects and analyzes Arcoxia side effect and adverse reports submitted by Arcoxia users, such as .

Summary

FDA Adverse Reports: 3. View All

Arcoxia FDA safety alerts: No

Reported hospitalizations: 3

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Often additional risks of using a medication, such as Arcoxia, 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 Arcoxia users, Learn more about unwanted side effects & find ways to reduce them. Browse Arcoxia Adverse Reports reported to FDA and participate in Arcoxia discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Arcoxia. 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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Arcoxia Adverse Effect Reports (FDA)

6313887-2 | Haemorrhage
on Aug 04, 2009 Male patient from GERMANY , 66 years of age, weighting 189.6 lb, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), atrial fibrillation (What is atrial fibrillation?), hyperuricaemia, blood folate decreased, prophylaxis against gastrointestinal ulcer, hypertension and was treated with Arcoxia (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhage. Arcoxia dosage: Zur Entlassung Immer Noch Pausiert. During the same period patient was treated with METEX (View Metex Review and Metex Label ), FALITHROM (View Falithrom Review and Falithrom Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), DECORTIN (Seit 2006 Reduziert (seit 2000) 1.5 - 0 - 0.5) (View Decortin Review and Decortin Label ), FOLSAEURE (View Folsaeure Review and Folsaeure Label ), PANTOZOL (View Pantozol Review and Pantozol Label ), RAMIPRIL (Ramipril 2.5mg ; Hct 12,5 Mg) (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

4940996-2 | Deep Vein Thrombosis, Fibrin D Dimer Increased
Patient was taking Arcoxia (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), fibrin d dimer increased on Jan 19, 2006 from ITALY Additional patient health information: Male patient , 53 years of age, was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), psoriatic arthropathy and. Arcoxia dosage: 90 Mg, Prn. During the same period patient was treated with SANDIMMUNE (50 Mg, Tid) (View Sandimmune Review and Sandimmune Label ). Patient was hospitalized.

4894874-8 | Deep Vein Thrombosis, Fibrin D Dimer Increased
Adverse event was reported on Jan 19, 2006 by a Male patient taking Arcoxia (View Usage) (Dosage: 90 Mg, Prn) was diagnosed with rheumatoid arthritis (What is rheumatoid arthritis?), psoriatic arthropathy and. Location: ITALY , 53 years of age, After Arcoxia was administered, patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), fibrin d dimer increased. During the same period patient was treated with SANDIMMUNE (50 Mg, Tid) (View Sandimmune Review and Sandimmune Label ). Patient was hospitalized.

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Arcoxia Questions, Answers, Feedback and Comments

Comments to date: 1. Page 1 of 1.

K Mayo-Smith Thailand	6:21am on Monday, January 2nd, 2012
Does Arcoxian have any adverse interaction with heart medications?

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 Arcoxia 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 Arcoxia quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Arcoxia 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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Deep Vein Thrombosis	What is Deep vein thrombosis?
Fibrin D Dimer Increased
Haemorrhage

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Arcoxia adverse events reported to FDA.

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Arcoxia Adverse Effect Reports (FDA)

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