Arthryl Side Effects

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Arthryl adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 2. View All

Arthryl FDA safety alerts: No

Reported hospitalizations: 2

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

5398856-1 | Bronchoscopy, C-reactive Protein Increased, Cardiac Failure, Dyspnoea, Hypotonia, Lung Disorder, Lung Infiltration, Pulmonary Oedema, White Blood Cell Count Increased
on Jul 23, 2007 Male patient from FINLAND , 68 years of age, was treated with Arthryl (View Usage). Patient experienced the following unwanted or unexpected effects: bronchoscopy, c-reactive protein increased, cardiac failure, dyspnoea, hypotonia, lung disorder, lung infiltration, pulmonary oedema, white blood cell count increased. Arthryl dosage: 1.5 G, Unk. During the same period patient was treated with ZOLT (15 Mg, Unk) (View Zolt Review and Zolt Label ), EMGESAN (250 Mg, Unk) (View Emgesan Review and Emgesan Label ), LITALGIN (View Litalgin Review and Litalgin Label ), MOBIC (7.5 Mg, Prn) (View Mobic Review and Mobic Label ), BURANA (600 Mg, Prn) (View Burana Review and Burana Label ), PANADOL FORTE (1 G, Prn) (View Panadol Forte Review and Panadol Forte Label ), PRIMASPAN (100 Mg, Unk) (View Primaspan Review and Primaspan Label ), OMEPRAZOLE (40 Mg/day) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5396541-3 | Bronchoscopy, C-reactive Protein Increased, Dyspnoea, Hypotonia, Lung Disorder, Lung Infiltration, Pulmonary Oedema, White Blood Cell Count Increased
Patient was taking Arthryl (View Usage). Patient had the following side effects: bronchoscopy, c-reactive protein increased, dyspnoea, hypotonia, lung disorder, lung infiltration, pulmonary oedema, white blood cell count increased on Jul 23, 2007 from FINLAND Additional patient health information: Male patient , 68 years of age, . Arthryl dosage: 1.5 G, Unk. During the same period patient was treated with ZOLT (15 Mg, Unk) (View Zolt Review and Zolt Label ), EMGESAN (250 Mg, Unk) (View Emgesan Review and Emgesan Label ), LITALGIN (View Litalgin Review and Litalgin Label ), MOBIC (7.5 Mg, Prn) (View Mobic Review and Mobic Label ), BURANA (600 Mg, Prn) (View Burana Review and Burana Label ), PANTOL (1 G, Prn) (View Pantol Review and Pantol Label ), PRIMASPAN (100 Mg, Unk) (View Primaspan Review and Primaspan Label ), OMEPRAZOLE (40 Mg/day) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

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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 Arthryl 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 Arthryl quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Arthryl 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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ARTHRYL Side Effects

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Bronchoscopy
C-reactive Protein Increased
Cardiac Failure
Dyspnoea
Hypotonia
Lung Disorder
Lung Infiltration
Pulmonary Oedema
White Blood Cell Count Increased

ARTHRYL Side Effects

Compare, Review and Rank Arthryl Side Effects

View Safety Poll Results

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Arthryl adverse events reported to FDA.

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Arthryl Adverse Effect Reports (FDA)

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Arthryl Reactions