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Flupenthixol adverse events reported to FDA.

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

Summary

FDA Adverse Reports: 3. View All

Flupenthixol FDA safety alerts: No

Reported hospitalizations: 3

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

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6905754-8 | Bradycardia, Metabolic Encephalopathy
on Jul 21, 2010 Female patient from UNITED KINGDOM , 41 years of age, was diagnosed with intentional overdose and was treated with Flupenthixol (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, metabolic encephalopathy. Flupenthixol dosage: . During the same period patient was treated with OXAZEPAM (View Oxazepam Review and Oxazepam Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ). Patient was hospitalized.

6905753-6 | Bradycardia, Metabolic Encephalopathy
Patient was taking Flupenthixol (View Usage). Patient had the following side effects: bradycardia, metabolic encephalopathy on Jul 21, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 41 years of age, was diagnosed with intentional overdose and. Flupenthixol dosage: . During the same period patient was treated with OXAZEPAM (View Oxazepam Review and Oxazepam Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ). Patient was hospitalized.

6905752-4 | Bradycardia, Metabolic Encephalopathy
Adverse event was reported on Jul 21, 2010 by a Female patient taking Flupenthixol (View Usage) (Dosage: ) was diagnosed with intentional overdose and. Location: UNITED KINGDOM , 41 years of age, After Flupenthixol was administered, patient had the following side effects: bradycardia, metabolic encephalopathy. During the same period patient was treated with OXAZEPAM (View Oxazepam Review and Oxazepam Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ). Patient was hospitalized.


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