Asphanate Side Effects

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Asphanate adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 2. View All

Asphanate FDA safety alerts: No

Reported deaths: 2

Reported hospitalizations: 2

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

5414348-5 | Cardiac Failure Congestive, Cardio-respiratory Arrest, Electrocardiogram Qt Prolonged, Implantable Defibrillator Malfunction, Supraventricular Extrasystoles, Ventricular Fibrillation, Ventricular Tachycardia
on Jul 31, 2007 Female patient from JAPAN , 73 years of age, was diagnosed with ventricular tachycardia and was treated with Asphanate (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac failure congestive, cardio-respiratory arrest, electrocardiogram qt prolonged, implantable defibrillator malfunction, supraventricular extrasystoles, ventricular fibrillation, ventricular tachycardia. Asphanate dosage: 81 Mg, 1x/day. During the same period patient was treated with SLOW K (800 Mg, 2x/day) (View Slow-k Review and Slow-k Label ), TEGRETOL (200 Mg, 3x/day) (View Tegretol Review and Tegretol Label ), ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), NIFEKALANT (15 Mg, Unk) (View Nifekalant Review and Nifekalant Label ). Patient was hospitalized.

5375465-1 | Cardiac Failure Congestive, Cardio-respiratory Arrest, Electrocardiogram Qt Prolonged, Implantable Defibrillator Malfunction, Supraventricular Extrasystoles, Ventricular Fibrillation, Ventricular Tachycardia
Patient was taking Asphanate (View Usage). Patient had the following side effects: cardiac failure congestive, cardio-respiratory arrest, electrocardiogram qt prolonged, implantable defibrillator malfunction, supraventricular extrasystoles, ventricular fibrillation, ventricular tachycardia on Jun 18, 2007 from JAPAN Additional patient health information: Female patient , 73 years of age, was diagnosed with ventricular tachycardia and. Asphanate dosage: 81 Mg, 1x/day. During the same period patient was treated with SLOW K (1200 Mg, 1x/day) (View Slow-k Review and Slow-k Label ), TEGRETOL (600 Mg, 1x/day) (View Tegretol Review and Tegretol Label ), ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), NIFEKALANT (15 Mg, Unk) (View Nifekalant Review and Nifekalant Label ). Patient was hospitalized.

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Asphanate Questions, Answers, Feedback and Comments

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

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Asphanate adverse events reported to FDA.

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Cardiac Failure Congestive
Cardio-respiratory Arrest
Electrocardiogram Qt Prolonged
Implantable Defibrillator Malfunction
Supraventricular Extrasystoles
Ventricular Fibrillation
Ventricular Tachycardia

ASPHANATE Side Effects

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Asphanate adverse events reported to FDA.

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Asphanate Adverse Effect Reports (FDA)

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Asphanate Reactions