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Rantudil adverse events reported to FDA.

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Summary

FDA Adverse Reports: 2. View All

Rantudil FDA safety alerts: No

Reported deaths: 2

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

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6636915-3 | Cardiac Failure, Cardiovascular Insufficiency, Gastrointestinal Disorder, Respiratory Failure, Upper Gastrointestinal Haemorrhage
on Mar 10, 2010 Female patient from GERMANY , 93 years of age, weighting 123.5 lb, was diagnosed with osteoarthritis (What is osteoarthritis?) and was treated with Rantudil (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure, cardiovascular insufficiency, gastrointestinal disorder, respiratory failure, upper gastrointestinal haemorrhage. Rantudil dosage: . During the same period patient was treated with FEBROFEN (View Febrofen Review and Febrofen Label ), MAJAMIL PROLONGATUM (View Majamil Prolongatum Review and Majamil Prolongatum Label ), ENARENAL (View Enarenal Review and Enarenal Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), KALIPOZ (View Kalipoz Review and Kalipoz Label ), BISOCARD (View Bisocard Review and Bisocard Label ), FUROSEMID (View Furosemid Review and Furosemid Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ).

6552012-X | Cardiovascular Insufficiency, Respiratory Failure, Respiratory Tract Haemorrhage
Patient was taking Rantudil (View Usage). Patient had the following side effects: cardiovascular insufficiency, respiratory failure, respiratory tract haemorrhage on Dec 31, 2009 from POLAND Additional patient health information: Female patient , 93 years of age, weighting 123.5 lb, was diagnosed with osteoarthritis (What is osteoarthritis?) and. Rantudil dosage: . During the same period patient was treated with FEBROFEN (View Febrofen Review and Febrofen Label ), MAJAMIL PROLONGATUM (View Majamil Prolongatum Review and Majamil Prolongatum Label ), ENARENAL (View Enarenal Review and Enarenal Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), KALIPOZ (View Kalipoz Review and Kalipoz Label ), BISOCARD (View Bisocard Review and Bisocard Label ), FUROSEMID (View Furosemid Review and Furosemid Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ).


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