Labetolol Side Effects

If You had Labetolol side effect, You are not alone. Other patients reported side effects.

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Labetolol adverse events reported to FDA.

Have You Experienced unusual Labetolol symptoms? PatientsVille.com collects and analyzes Labetolol side effect and adverse reports submitted by Labetolol users, such as I re-introduced some hydralazine (25 mg tablets)|.

Summary

FDA Adverse Reports: 2. View All

Labetolol FDA safety alerts: No

Reported hospitalizations: 1

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I re-introduced some hydralazine (25 mg tablets)

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

6272443-5 | Anaemia, Blood Potassium Increased, Blood Pressure Increased, Post Procedural Haemorrhage, Proteinuria
on Jul 10, 2009 Male patient from UNITED STATES , 55 years of age, weighting 176.0 lb, was treated with Labetolol (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, blood potassium increased, blood pressure increased, post procedural haemorrhage, proteinuria. Labetolol dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PROCARDIA (View Procardia Review and Procardia Label ), NEXIUM (View Nexium Review and Nexium Label ), LIPITOR (View Lipitor Review and Lipitor Label ), NORVASC (View Norvasc Review and Norvasc Label ), IMDUR (View Imdur Review and Imdur Label ), SLOW FE IRON (View Slow Fe Iron Review and Slow Fe Iron Label ). Patient was hospitalized.

4732495-8 | Atrioventricular Block, Blood Pressure Inadequately Controlled, Blood Pressure Increased, Cardiac Arrest, Cardiac Failure Congestive, Cerebrovascular Accident, Condition Aggravated, Renal Artery Stenosis
Patient was taking Labetolol (View Usage). Patient had the following side effects: atrioventricular block, blood pressure inadequately controlled, blood pressure increased, cardiac arrest (What is cardiac arrest?), cardiac failure congestive, cerebrovascular accident, condition aggravated, renal artery stenosis on Aug 01, 2005 from UNITED STATES Additional patient health information: Male patient , 59 years of age, weighting 195.1 lb, was diagnosed with hypertension, atrial fibrillation (What is atrial fibrillation?) and. Labetolol dosage: 200 Mg Po Bid. During the same period patient was treated with VERAPAMIL (240 Mg Po Bid) (View Verapamil Review and Verapamil 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 Labetolol 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 Labetolol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Labetolol 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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	Yes, Moderate
	Yes, Minor
	No

	Exceeded Expectations
	Effective
	Somewhat Effective
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LABETOLOL Side Effects

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Labetolol adverse events reported to FDA.

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Labetolol Adverse Effect Reports (FDA)

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Labetolol Reactions

Anaemia
Atrioventricular Block
Blood Potassium Increased
Blood Pressure Inadequately Controlled
Blood Pressure Increased
Cardiac Arrest	What is Cardiac arrest?
Cardiac Failure Congestive
Cerebrovascular Accident
Condition Aggravated
Post Procedural Haemorrhage
Proteinuria
Renal Artery Stenosis

LABETOLOL Side Effects

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Labetolol adverse events reported to FDA.

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Labetolol Adverse Effect Reports (FDA)

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Labetolol Reactions