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Betaserc Side Effects

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Common Betaserc Side Effects


The most commonly reported Betaserc side effects (click to view or check a box to report):

Vomiting (2)
Atrioventricular Block Second Degree (1)
Apathy (1)
Hepatic Cyst (1)
Blood Alkaline Phosphatase Increased (1)
Cholestatic Liver Injury (1)
Fatigue (1)
Convulsion (1)
Confusional State (1)
Hypertension (1)
Skin Odour Abnormal (1)
Lower Limb Fracture (1)
Loss Of Consciousness (1)
Incorrect Dose Administered (1)
Micturition Frequency Decreased (1)
Paraesthesia (1)
Sense Of Oppression (1)
Sciatica (1)
Rhabdomyolysis (1)
Somnolence (1)

➢ More



If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Betaserc Side Effects Reported to FDA



Betaserc Side Effect Report#8444457-8
Cholestatic Liver Injury, Gamma-glutamyltransferase Increased, Blood Alkaline Phosphatase Increased
This is a report of a 84-year-old male patient (weight: NA) from Switzerland, suffering from the following health symptoms/conditions: NA, who was treated with Betaserc (dosage: NA, start time:
Feb 03, 2012), combined with:
  • Acetaminophen
  • Rocephin
  • Amlodipin Actavis
  • Zoloft
  • Nexium
  • Mycostatin
  • Haldol
  • Ferinject
and developed a serious reaction and side effect(s): Cholestatic Liver Injury, Gamma-glutamyltransferase Increased, Blood Alkaline Phosphatase Increased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Betaserc treatment in male patients, resulting in Cholestatic Liver Injury side effect.
Betaserc Side Effect Report#8376388-6
Transient Ischaemic Attack, Paraesthesia, Skin Odour Abnormal, Loss Of Consciousness, Somnolence, Confusional State, Fatigue, Apathy, Hepatic Cyst
This report suggests a potential Betaserc Transient Ischaemic Attack side effect(s) that can have serious consequences. A 78-year-old female patient (weight: NA) from Croatia (local Name: Hrvatska) was diagnosed with the following symptoms/conditions: deafness,diabetes mellitus and used Betaserc (dosage: NA) starting
Jan 01, 2004. After starting Betaserc the patient began experiencing various side effects, including: Transient Ischaemic Attack, Paraesthesia, Skin Odour Abnormal, Loss Of Consciousness, Somnolence, Confusional State, Fatigue, Apathy, Hepatic CystAdditional drugs used concurrently:
  • Glurenorm (1 Df, Qd)
  • Hydrochlorothiazide W/cilazapril
  • Moduretic 5-50 (1 Df, Qd)
  • Bisoprolol Fumarate (1 Df, Qd)
The patient was hospitalized. Although Betaserc demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Transient Ischaemic Attack, may still occur.
Betaserc Side Effect Report#8376018-3
Convulsion, Sciatica, Headache
This Convulsion problem was reported by a consumer or non-health professional from Brazil. A female patient (weight: NA) was diagnosed with the following symptoms/conditions: dizziness,insomnia,blood cholesterol increased,convulsion. On NS this consumer started treatment with Betaserc (dosage: 1 Df, A Day). The following drugs were being taken at the same time:
  • Clonazepam (0.25 Mg, At Night)
  • Simvastatin (1 Df, At Night)
  • Phenytoin
  • Trileptal (2 Df, (1 Tablet In The Morning And 1 Tablet At Night))
  • Trileptal (2 Df, (1 Tablet In The Morning And 1 Tablet At Night))
When using Betaserc, the patient experienced the following unwanted symptoms/side effects: Convulsion, Sciatica, HeadacheAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Convulsion, may become evident only after a product is in use by the general population.
Betaserc Side Effect Report#8133684-5
Atrioventricular Block Second Degree, Heart Rate Decreased, Sense Of Oppression
This Atrioventricular Block Second Degree side effect was reported by a physician from France. A 50-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Betaserc (drug dosage: Unk Ukn, Unk), which was initiated on
Jan 17, 2012. Concurrently used drugs:
  • Ditropan (Unk Ukn, Unk)
  • Trospium Chloride (Unk Ukn, Unk)
  • Gilenya (0.5 Mg, Daily)
  • Lyrica (Unk Ukn, Unk)
  • Tanganil (Unk Ukn, Unk)
.After starting to take Betaserc the consumer reported adverse symptoms, such as: Atrioventricular Block Second Degree, Heart Rate Decreased, Sense Of OppressionThese side effects may potentially be related to Betaserc. The patient was hospitalized.
Betaserc Side Effect Report#7544065-7
Hypertension, Micturition Frequency Decreased
This is a report of a 67-year-old male patient (weight: NA) from Brazil, suffering from the following health symptoms/conditions: ear disorder, who was treated with Betaserc (dosage: 1 Tablet, Qd, start time: NS), combined with:
  • Aspirin
  • Ancoron
  • Insulin (30 Cc)
  • Diovan (160 Mg, Qd)
  • Sinvacor (1 Tablet, Qd)
and developed a serious reaction and side effect(s): Hypertension, Micturition Frequency Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Betaserc treatment in male patients, resulting in Hypertension side effect. The patient was hospitalized.
Betaserc Side Effect Report#7371722-8
Lower Limb Fracture
This report suggests a potential Betaserc Lower Limb Fracture side effect(s) that can have serious consequences. A 65-year-old female patient (weight: NA) from Switzerland was diagnosed with the following symptoms/conditions: meniere's disease,ophthalmologic treatment,osteoporosis and used Betaserc (dosage: NA) starting
Jan 01, 2004. After starting Betaserc the patient began experiencing various side effects, including: Lower Limb FractureAdditional drugs used concurrently:
  • Acular
  • Fosamax
  • Calcimagon D3
  • Nexium
  • Vitamine A
  • Boniva
  • Protagent
  • Lacrycon
The patient was hospitalized. Although Betaserc demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Lower Limb Fracture, may still occur.
Betaserc Side Effect Report#5146959-9
Vomiting
This Vomiting problem was reported by a health professional from . A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jul 07, 2006 this consumer started treatment with Betaserc (dosage: NA). The following drugs were being taken at the same time:
  • Zoxon
  • Penester
  • Oxaliplatin
  • Leucovorin Calcium
  • Fluorouracil (400 Mg/m?, Iv Bolus D1+d2 Followed By 5-fu 2400 Mg/m? Over 46-hour Continuous Infusion.)
When using Betaserc, the patient experienced the following unwanted symptoms/side effects: VomitingThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Vomiting, may become evident only after a product is in use by the general population.
Betaserc Side Effect Report#5143540-2
Incorrect Dose Administered, Rhabdomyolysis
This Incorrect Dose Administered side effect was reported by a physician from Switzerland. A 60-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Betaserc (drug dosage: NA), which was initiated on
Feb 28, 2006. Concurrently used drugs:
  • Beloc
  • Neurontin
  • Prednisone Tab
  • Cellcept
  • Aspirin
  • Pantozol
  • Sandimmune
  • Plavix
.After starting to take Betaserc the consumer reported adverse symptoms, such as: Incorrect Dose Administered, RhabdomyolysisThese side effects may potentially be related to Betaserc. The patient was hospitalized.
Betaserc Side Effect Report#5142496-6
Vomiting
This is a report of a male patient (weight: NA) from , suffering from the following health symptoms/conditions: NA, who was treated with Betaserc (dosage: NA, start time:
Jul 07, 2006), combined with:
  • Zoxon
  • Penester
  • Oxaliplatin
  • Leucovorin
  • Fluorouracil (400 Mg/m?, Iv Bolus D1+d2 Followed By 5-fu 2400 Mg/m? Over 46-hour Continuous Infusion.)
and developed a serious reaction and side effect(s): Vomiting after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Betaserc treatment in male patients, resulting in Vomiting side effect. The patient was hospitalized.



The appearance of Betaserc on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.


Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Betaserc reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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