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Maintate Side Effects

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Common Maintate Side Effects


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

Interstitial Lung Disease (2)
Treatment Noncompliance (1)
Thrombocytopenia (1)
Syncope (1)
Urticaria (1)
Hepatic Function Abnormal (1)
Cataract (1)
Low Density Lipoprotein Increased (1)
Liver Disorder (1)
Swelling (1)
Nephrogenic Anaemia (1)
Oedema Peripheral (1)
Nodal Rhythm (1)
Blood Creatinine Increased (1)
Oliguria (1)
Blood Pressure Diastolic Decreased (1)
Bradycardia (1)
Blood Pressure Systolic Increased (1)
Blood Pressure Increased (1)
Megakaryocytes Decreased (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.

Maintate Side Effects Reported to FDA



Maintate Side Effect Report#8934649
Interstitial Lung Disease
This is a report of a 71-year-old female patient (weight: NA) from JP, suffering from the following health symptoms/conditions: supraventricular extrasystoles, who was treated with Maintate (dosage: NA, start time:
May 09, 2012), combined with:
  • Bufferin 81mg
  • Gaslon N
  • Gasmotin
  • Simponi
  • Natrix
  • Diovan
  • Norvasc
  • Sunrythm
and developed a serious reaction and side effect(s): Interstitial Lung Disease after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Maintate treatment in female patients, resulting in Interstitial Lung Disease side effect. The patient was hospitalized.
Maintate Side Effect Report#7415114-1
Diabetic Nephropathy, Blood Pressure Systolic Increased, Glycosylated Haemoglobin Increased, Urticaria, Blood Pressure Diastolic Decreased, Nephrogenic Anaemia, Swelling, Oedema Peripheral, Cough
This report suggests a potential Maintate Diabetic Nephropathy side effect(s) that can have serious consequences. A female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: hypertension and used Maintate (dosage: 2.5 Mg, Unk) starting
Aug 06, 2008. After starting Maintate the patient began experiencing various side effects, including: Diabetic Nephropathy, Blood Pressure Systolic Increased, Glycosylated Haemoglobin Increased, Urticaria, Blood Pressure Diastolic Decreased, Nephrogenic Anaemia, Swelling, Oedema Peripheral, CoughAdditional drugs used concurrently:
  • Novorapid (46 Iu, Unk)
  • Zetia (10 Mg, Unk)
  • Artist (Unk)
  • Valsartan (80 Mg Per Day)
  • Lantus (32 Iu Daily)
  • Diart (30 Mg, Unk)
  • Benecid (500 Mg, Unk)
  • Lipitor (20 Mg, Unk)
The patient was hospitalized. Although Maintate demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Diabetic Nephropathy, may still occur.
Maintate Side Effect Report#7325571-7
Syncope
This Syncope problem was reported by a physician from Japan. A 66-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension,rhinitis allergic. On
Mar 06, 2007 this consumer started treatment with Maintate (dosage: NA). The following drugs were being taken at the same time:
  • Fexofenadine Hcl (Dose Unit: 60 Mg)
  • Sinlestal
  • Gaster D (Dose Unit: 10 Mg)
When using Maintate, the patient experienced the following unwanted symptoms/side effects: SyncopeAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Syncope, may become evident only after a product is in use by the general population.
Maintate Side Effect Report#7310732-3
Interstitial Lung Disease, Low Density Lipoprotein Increased, Cataract
This Interstitial Lung Disease side effect was reported by a pharmacist from Japan. A 80-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Maintate (drug dosage: Unk), which was initiated on NS. Concurrently used drugs:
  • Bufferin (81 Mg, Unk)
  • Lochol (30 Mg, Daily)
.After starting to take Maintate the consumer reported adverse symptoms, such as: Interstitial Lung Disease, Low Density Lipoprotein Increased, CataractThese side effects may potentially be related to Maintate. The patient was hospitalized.
Maintate Side Effect Report#7207242-0
Hepatic Function Abnormal
This is a report of a 88-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Maintate (dosage: Unk, start time:
Sep 17, 2010), combined with:
  • Lipitor (10 Mg, 1x/day)
  • Gaster (20 Mg, 1x/day)
  • Thyradin S (Unk)
  • Risedronate Sodium (Unk)
  • Pletal (400 Mg, 1x/day)
  • Senevacul (Unk)
  • Selbex (Unk)
  • Predonine (Unk)
and developed a serious reaction and side effect(s): Hepatic Function Abnormal after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Maintate treatment in female patients, resulting in Hepatic Function Abnormal side effect. The patient was hospitalized.
Maintate Side Effect Report#6060151-5
Liver Disorder
This report suggests a potential Maintate (bisoprolol Fumarate) Liver Disorder side effect(s) that can have serious consequences. A 62-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Maintate (bisoprolol Fumarate) (dosage: Daily Dose) starting
Jun 01, 2007. After starting Maintate (bisoprolol Fumarate) the patient began experiencing various side effects, including: Liver DisorderAdditional drugs used concurrently: NA. Although Maintate (bisoprolol Fumarate) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Liver Disorder, may still occur.
Maintate Side Effect Report#5713844-0
Blood Creatinine Increased, Continuous Haemodiafiltration, Oliguria, Pleural Effusion, Pulmonary Congestion, Renal Failure, Shock, Somnolence
This Blood Creatinine Increased problem was reported by a consumer or non-health professional from Japan. A 39-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Maintate (bisoprlol Fumarate) (dosage: 150 Mg (150 Mg, 1 In 1 D)). The following drugs were being taken at the same time:
  • Amlodipine (850 Mg (850 Mg, 1 In 1 D))
When using Maintate (bisoprlol Fumarate), the patient experienced the following unwanted symptoms/side effects: Blood Creatinine Increased, Continuous Haemodiafiltration, Oliguria, Pleural Effusion, Pulmonary Congestion, Renal Failure, Shock, SomnolenceThe 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 Blood Creatinine Increased, may become evident only after a product is in use by the general population.
Maintate Side Effect Report#5661617-X
Anti-platelet Antibody Positive, Bleeding Time Prolonged, Blood Pressure Increased, Epistaxis, Haemoptysis, Haemorrhage Subcutaneous, Megakaryocytes Decreased, Platelet Count Decreased, Thrombocytopenia
This Anti-platelet Antibody Positive side effect was reported by a physician from Japan. A 68-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension,lipids abnormal.The patient was prescribed Maintate (drug dosage: 2.5 Mg/day), which was initiated on
Jun 01, 2005. Concurrently used drugs:
  • Fluvastatin (30mg/day)
  • Norvasc (5mg/day)
  • Aspirin (100mg/day)
  • Diovan (160 Mg/day)
  • Depas (1 Mg/day)
.After starting to take Maintate the consumer reported adverse symptoms, such as: Anti-platelet Antibody Positive, Bleeding Time Prolonged, Blood Pressure Increased, Epistaxis, Haemoptysis, Haemorrhage Subcutaneous, Megakaryocytes Decreased, Platelet Count Decreased, ThrombocytopeniaThese side effects may potentially be related to Maintate. The patient was hospitalized.
Maintate Side Effect Report#4701504-4
Atrial Fibrillation, Bradycardia, Disease Recurrence, Fall, Nodal Rhythm, Sinus Arrest, Treatment Noncompliance
This is a report of a 56-year-old female patient (weight: NA) from , suffering from the following health symptoms/conditions: atrial fibrillation,hypertension, who was treated with Maintate (tablet) (bisoprolol Fumarate) (dosage: 2.5 Mg (2,5 Mg, 1 In 1 D), Oral, start time:
May 10, 2005), combined with: NA. and developed a serious reaction and side effect(s): Atrial Fibrillation, Bradycardia, Disease Recurrence, Fall, Nodal Rhythm, Sinus Arrest, Treatment Noncompliance after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Maintate (tablet) (bisoprolol Fumarate) treatment in female patients, resulting in Atrial Fibrillation side effect. The patient was hospitalized.



The appearance of Maintate 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.

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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.

    Maintate 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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    Maintate Safety Alerts, Active Ingredients, Usage Information

    More About Maintate

    Side Effects reported to FDA: 9

    Maintate safety alerts: No

    Reported hospitalizations: 5

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