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Lopresor adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Lopresor FDA safety alerts: No

Reported hospitalizations: 3

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

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6322828-3 | Acute Myocardial Infarction, Angina Unstable, Arrhythmia Supraventricular, Arterial Stenosis, Blood Cholesterol Increased, Blood Creatine Phosphokinase Increased, Blood Creatine Phosphokinase Mb, Blood Triglycerides Increased, Caesarean Section
on Aug 17, 2009 Female patient from UNITED STATES , 42 years of age, was treated with Lopresor (View Usage). Patient experienced the following unwanted or unexpected effects: acute myocardial infarction, angina unstable, arrhythmia supraventricular, arterial stenosis, blood cholesterol increased, blood creatine phosphokinase increased, blood creatine phosphokinase mb, blood triglycerides increased, caesarean section. Lopresor dosage: Unk. During the same period patient was treated with ASPIRIN (81 Mg, Qd) (View Aspirin Review and Aspirin Label ), HEPARIN (View Heparin Review and Heparin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), LABETALOL HCL (50 Mg, Bid) (View Labetalol Hcl Review and Labetalol Hcl Label ), CLOPIDOGREL (600 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ). Patient was hospitalized.

6318581-X | Bradycardia, Hypotension, Liver Disorder, Sinus Arrest
Patient was taking Lopresor (View Usage). Patient had the following side effects: bradycardia, hypotension, liver disorder, sinus arrest on Aug 19, 2009 from JAPAN Additional patient health information: Male patient , weighting 110.2 lb, was diagnosed with pulse abnormal and. Lopresor dosage: 40 Mg, Prn. During the same period patient was treated with HISHIMIDON (100 Mg, Unk) (View Hishimidon Review and Hishimidon Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), HALCION (0.125 Mg, Unk) (View Halcion Review and Halcion Label ), TAKEPRON (15 Mg, Unk) (View Takepron Review and Takepron Label ), FRANDOL S (40 Mg, Qd) (View Frandol S Review and Frandol S Label ), NITOROL (40 Mg, Unk) (View Nitorol Review and Nitorol Label ), ANPLAG (300 Mg, Unk) (View Anplag Review and Anplag Label ).

6318562-6 | Premature Baby, Small For Dates Baby
Adverse event was reported on Aug 17, 2009 by a Female patient taking Lopresor (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 3.53 lb, After Lopresor was administered, patient had the following side effects: premature baby, small for dates baby. During the same period patient was treated with ASPIRIN (81 Mg, Qd) (View Aspirin Review and Aspirin Label ), HEPARIN (View Heparin Review and Heparin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), LABETALOL HCL (50 Mg, Bid) (View Labetalol Hcl Review and Labetalol Hcl Label ), CLOPIDOGREL (600 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), RAMIPRIL (2.5 Mg, Unk) (View Ramipril Review and Ramipril Label ).

6317743-5 | Premature Baby, Small For Dates Baby
on Aug 17, 2009 Female patient from UNITED STATES , weighting 3.70 lb, was treated with Lopresor (View Usage). Patient experienced the following unwanted or unexpected effects: premature baby, small for dates baby. Lopresor dosage: . During the same period patient was treated with ASPIRIN (81 Mg, Qd) (View Aspirin Review and Aspirin Label ), HEPARIN (View Heparin Review and Heparin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), CLOPIDOGREL (600 Mg, Unk) (View Clopidogrel Review and Clopidogrel Label ), LABETALOL HCL (50 Mg, Bid) (View Labetalol Hcl Review and Labetalol Hcl Label ), RAMIPRIL (2.5 Mg, Unk) (View Ramipril Review and Ramipril Label ).


6306289-6 | Bradycardia, Hypotension, Sinus Arrest
on Aug 07, 2009 Male patient from JAPAN , weighting 110.2 lb, was diagnosed with pulse abnormal and was treated with Lopresor (View Usage). Patient had the following side effects: bradycardia, hypotension, sinus arrest. Lopresor dosage: 40 Mg, Prn. During the same period patient was treated with HISHIMIDON (100 Mg, Unk) (View Hishimidon Review and Hishimidon Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), HALCION (0.125 Mg, Unk) (View Halcion Review and Halcion Label ), TAKEPRON (15 Mg, Unk) (View Takepron Review and Takepron Label ), SIGMART (15 Mg, Unk) (View Sigmart Review and Sigmart Label ), FRANDOL (1 Df, Tid) (View Frandol Review and Frandol Label ), NITOROL (40 Mg, Unk) (View Nitorol Review and Nitorol Label ), ANPLAG (300 Mg, Unk) (View Anplag Review and Anplag Label ).

6284293-4 | Bradycardia, Cardiac Arrest
Patient was taking Lopresor (View Usage). After Lopresor was administered, patient had the following side effects: bradycardia, cardiac arrest (What is cardiac arrest?) on Jul 22, 2009 from JAPAN Additional patient health information: Male patient , 67 years of age, was diagnosed with pulse abnormal and. Lopresor dosage: 40 Mg, Prn. During the same period patient was treated with HISHIMIDON (100 Mg, Unk) (View Hishimidon Review and Hishimidon Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), HALCION (0.125 Mg, Unk) (View Halcion Review and Halcion Label ), TAKEPRON (15 Mg, Unk) (View Takepron Review and Takepron Label ), SIGMART (15 Mg, Unk) (View Sigmart Review and Sigmart Label ), FRANDOL (1 Df, Tid) (View Frandol Review and Frandol Label ), NITOROL (40 Mg, Unk) (View Nitorol Review and Nitorol Label ), ANPLAG (300 Mg, Unk) (View Anplag Review and Anplag Label ).

6125936-5 | Intentional Overdose, Suicide Attempt
Adverse event was reported on Aug 09, 2008 by a Male patient taking Lopresor (View Usage) (Dosage: 15 Df) . Location: JAPAN , 47 years of age, Patient experienced the following unwanted or unexpected effects: intentional overdose, suicide attempt.

6054292-6 | Prostatic Disorder
on Jan 16, 2009 Male patient from MEXICO , 70 years of age, was diagnosed with hypertension and was treated with Lopresor (View Usage). Patient had the following side effects: prostatic disorder. Lopresor dosage: 100 Mg, Qd. During the same period patient was treated with SELOKEN ZOC (Unk, Unk) (View Seloken Zoc Review and Seloken Zoc Label ).

6042123-X | Myoclonus, Vomiting
on Jan 09, 2009 Male patient from JAPAN , 64 years of age, was diagnosed with nasopharyngitis and was treated with Lopresor (View Usage). After Lopresor was administered, patient had the following side effects: myoclonus, vomiting. Lopresor dosage: . During the same period patient was treated with DEXTROMETHORPHAN HYDROBROMIDE (30 Mg/day) (View Dextromethorphan Hydrobromide Review and Dextromethorphan Hydrobromide Label ). Patient was hospitalized.

6030803-1 | Myoclonus, Vomiting
Patient was taking Lopresor (View Usage). Patient experienced the following unwanted or unexpected effects: myoclonus, vomiting on Dec 24, 2008 from JAPAN Additional patient health information: Male patient , 64 years of age, was diagnosed with nasopharyngitis and. Lopresor dosage: . During the same period patient was treated with DEXTROMETHORPHAN HYDROBROMIDE (30 Mg/day) (View Dextromethorphan Hydrobromide Review and Dextromethorphan Hydrobromide 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 Lopresor 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 Lopresor quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Lopresor 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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Lopresor Reactions
Acute Myocardial Infarction
Angina Unstable
Arrhythmia Supraventricular
Arterial Stenosis
Blood Cholesterol Increased
Blood Creatine Phosphokinase Increased
Blood Creatine Phosphokinase Mb
Blood Triglycerides Increased
Bradycardia
Caesarean Section
Cardiac ArrestWhat is Cardiac arrest?
Hypotension
Intentional Overdose
Liver Disorder
Myoclonus
Premature Baby
Prostatic Disorder
Sinus Arrest
Small For Dates Baby
Suicide Attempt
Vomiting
Lopresor 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 Lopresor 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!