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Betaxolol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 7. View All

Betaxolol FDA safety alerts: No

Reported hospitalizations: 4

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

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6187538-4 | Feeling Abnormal, Loss Of Consciousness, Memory Impairment, Sinus Arrest
on Apr 30, 2009 Male patient from CZECH REPUBLIC , 58 years of age, was diagnosed with hypertension, hyperlipidaemia and was treated with Betaxolol (View Usage). Patient experienced the following unwanted or unexpected effects: feeling abnormal, loss of consciousness, memory impairment, sinus arrest. Betaxolol dosage: . During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

5913462-5 | Hypophagia, Nausea
Patient was taking Betaxolol (View Usage). Patient had the following side effects: hypophagia, nausea (What is nausea?) on Oct 08, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 136.0 lb, was diagnosed with supraventricular tachycardia and. Betaxolol dosage: 1/2 Tab In Am, 1/4 Tab In Pm Po.

5452245-X | Anxiety, Asthenia, Balance Disorder, Condition Aggravated, Dizziness, Eye Disorder, Eye Swelling, Fatigue, Gait Disturbance
Adverse event was reported on Sep 12, 2007 by a Female patient taking Betaxolol (View Usage) (Dosage: 1 Daily) was diagnosed with hypertension and. Location: UNITED STATES , 70 years of age, weighting 173.0 lb, After Betaxolol was administered, patient had the following side effects: anxiety (What is anxiety?), asthenia, balance disorder, condition aggravated, dizziness (What is dizziness?), eye disorder, eye swelling, fatigue, gait disturbance. Patient was hospitalized and became disabled.

5363831-X | Cardiogenic Shock, Intentional Overdose, Ventricular Hypokinesia
on Jun 08, 2007 Female patient from FRANCE , 38 years of age, was diagnosed with intentional overdose and was treated with Betaxolol (View Usage). Patient experienced the following unwanted or unexpected effects: cardiogenic shock, intentional overdose, ventricular hypokinesia. Betaxolol dosage: 5.32 G. During the same period patient was treated with ALCOHOL (Unk) (View Alcohol Review and Alcohol Label ), LORAZEPAM (30 G) (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.


5351076-9 | Cardiogenic Shock, Intentional Overdose, Ventricular Hypokinesia
on May 29, 2007 Female patient from FRANCE , 38 years of age, was diagnosed with intentional overdose and was treated with Betaxolol (View Usage). Patient had the following side effects: cardiogenic shock, intentional overdose, ventricular hypokinesia. Betaxolol dosage: 5.32 G.

4638540-2 | Eye Irritation, Instillation Site Irritation
Patient was taking Betaxolol (View Usage). After Betaxolol was administered, patient had the following side effects: eye irritation, instillation site irritation on Apr 18, 2005 from Additional patient health information: Female patient , 95 years of age, was diagnosed with open angle glaucoma and. Betaxolol dosage: Bid Ou. During the same period patient was treated with AZOPT (Bid Ou) (View Azopt Review and Azopt Label ).

4619289-9 | Loss Of Consciousness
Adverse event was reported on Mar 18, 2005 by a Female patient taking Betaxolol (View Usage) (Dosage: 10 Mg Po Qd [prior To Admission]) was diagnosed with hypertension and. Location: , weighting 168.0 lb, Patient experienced the following unwanted or unexpected effects: loss of consciousness. During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), LIQUID KCL (View Liquid Kcl Review and Liquid Kcl Label ), AXID (View Axid Review and Axid Label ), TUMS (View Tums Review and Tums 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 Betaxolol 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 Betaxolol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Betaxolol 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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Betaxolol Reactions
AnxietyWhat is Anxiety?
Asthenia
Balance Disorder
Cardiogenic Shock
Condition Aggravated
DizzinessWhat is Dizziness?
Eye Disorder
Eye Irritation
Eye Swelling
Fatigue
Feeling Abnormal
Gait Disturbance
Hypophagia
Instillation Site Irritation
Intentional Overdose
Loss Of Consciousness
Memory Impairment
NauseaWhat is Nausea?
Sinus Arrest
Ventricular Hypokinesia
Betaxolol Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Betaxolol adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!