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Artotec adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Artotec FDA safety alerts: No

Reported hospitalizations: 2

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

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6654369-8 | Rash Morbilliform
on Mar 15, 2010 Female patient from FRANCE , 76 years of age, was diagnosed with osteoarthritis (What is osteoarthritis?), pain (What is pain?) and was treated with Artotec (View Usage). Patient experienced the following unwanted or unexpected effects: rash morbilliform. Artotec dosage: Unk. During the same period patient was treated with IXPRIM (Unk) (View Ixprim Review and Ixprim Label ). Patient was hospitalized.

6453477-4 | Haematoma, International Normalised Ratio Increased
Patient was taking Artotec (View Usage). Patient had the following side effects: haematoma, international normalised ratio increased on Nov 13, 2009 from FRANCE Additional patient health information: Female patient , 80 years of age, . Artotec dosage: Unk. During the same period patient was treated with KETOPROFEN (Unk) (View Ketoprofen Review and Ketoprofen Label ), PREVISCAN (Unk) (View Previscan Review and Previscan Label ), TRAMADOL (150 Mg, 1x/day) (View Tramadol Review and Tramadol Label ), CRESTOR (5 Mg, Unk) (View Crestor Review and Crestor Label ), COVERSYL (5 Mg, Unk) (View Coversyl Review and Coversyl Label ), LASILIX (20 Mg, Unk) (View Lasilix Review and Lasilix Label ), DAFLON (500 Mg, Unk) (View Daflon Review and Daflon Label ), LERCANIDIPINE (20 Mg, Unk) (View Lercanidipine Review and Lercanidipine 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 Artotec 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 Artotec quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Artotec 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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How Did You Deal with Side Effects?

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Artotec Reactions
Haematoma
International Normalised Ratio Increased
Rash Morbilliform
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