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Rythmodan Side Effects

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Common Rythmodan Side Effects


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

Hypoglycaemia (5)
Ventricular Tachycardia (3)
Renal Disorder (3)
Hypoglycaemic Coma (2)
Dehydration (2)
Pneumonia Aspiration (2)
Disseminated Intravascular Coagulation (2)
Hypokalaemia (2)
Renal Impairment (2)
Stress Cardiomyopathy (2)
Sepsis (2)
Respiratory Paralysis (2)
Syncope (1)
Metabolic Alkalosis (1)
Condition Aggravated (1)
Electrocardiogram Qt Prolonged (1)
Hypovolaemia (1)


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.

Rythmodan Side Effects Reported to FDA



Rythmodan Side Effect Report#8897126
Metabolic Alkalosis, Syncope, Hypokalaemia, Electrocardiogram Qt Prolonged, Ventricular Tachycardia
This is a report of a 82-year-old female patient (weight: NA) from JP, suffering from the following health symptoms/conditions: NA, who was treated with Rythmodan (dosage: NA, start time: NS), combined with:
  • Lasix
  • Mexitil
  • Shakuyakukanzoutou
and developed a serious reaction and side effect(s): Metabolic Alkalosis, Syncope, Hypokalaemia, Electrocardiogram Qt Prolonged, Ventricular Tachycardia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rythmodan treatment in female patients, resulting in Metabolic Alkalosis side effect. The patient was hospitalized.
Rythmodan Side Effect Report#5360431-2
Disseminated Intravascular Coagulation, Hypokalaemia, Respiratory Paralysis, Sepsis, Stress Cardiomyopathy, Ventricular Tachycardia
This report suggests a potential Rythmodan /00271801/ Disseminated Intravascular Coagulation side effect(s) that can have serious consequences. A 79-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: NA and used Rythmodan /00271801/ (dosage: NA) starting
Nov 18, 2006. After starting Rythmodan /00271801/ the patient began experiencing various side effects, including: Disseminated Intravascular Coagulation, Hypokalaemia, Respiratory Paralysis, Sepsis, Stress Cardiomyopathy, Ventricular TachycardiaAdditional drugs used concurrently:
  • Lasix
  • Predonine /00016201/
  • Predonine /00016201/
  • Ambenonium Chloride
  • Aspara K /00466902/
Although Rythmodan /00271801/ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Disseminated Intravascular Coagulation, may still occur.
Rythmodan Side Effect Report#5329880-2
Disseminated Intravascular Coagulation, Respiratory Paralysis, Sepsis, Stress Cardiomyopathy, Ventricular Tachycardia
This Disseminated Intravascular Coagulation problem was reported by a physician from Japan. A 79-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Nov 18, 2006 this consumer started treatment with Rythmodan /00271801/ (dosage: NA). The following drugs were being taken at the same time:
  • Furosemide
  • Ambenonium Chloride
  • Predonine /00016201/
  • Predonine /00016201/
  • Aspara K /00466902/
When using Rythmodan /00271801/, the patient experienced the following unwanted symptoms/side effects: Disseminated Intravascular Coagulation, Respiratory Paralysis, Sepsis, Stress Cardiomyopathy, Ventricular TachycardiaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Disseminated Intravascular Coagulation, may become evident only after a product is in use by the general population.
Rythmodan Side Effect Report#5101459-7
Hypoglycaemia, Renal Disorder
This Hypoglycaemia side effect was reported by a pharmacist from Japan. A 53-year-old female patient (weight:NA) experienced the following symptoms/conditions: supraventricular tachycardia,iron deficiency,azotaemia,hypertension.The patient was prescribed Rythmodan (drug dosage: NA), which was initiated on
Nov 01, 2000. Concurrently used drugs:
  • Ferromia
  • Kremezin
  • Cardenalin
  • Adalat
  • Depas
  • Cozaar
  • Calcium Carbonate
  • Bufferin
.After starting to take Rythmodan the consumer reported adverse symptoms, such as: Hypoglycaemia, Renal DisorderThese side effects may potentially be related to Rythmodan. The patient was hospitalized.
Rythmodan Side Effect Report#5090122-7
Hypoglycaemia, Renal Disorder
This is a report of a 53-year-old female patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: supraventricular tachycardia,iron deficiency,azotaemia,hypertension, who was treated with Rythmodan (dosage: NA, start time:
Nov 01, 2000), combined with:
  • Ferromia
  • Kremezin
  • Cardenalin
  • Adalat
  • Depas
  • Cozaar
  • Calcium Carbonate
  • Bufferin
and developed a serious reaction and side effect(s): Hypoglycaemia, Renal Disorder after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Rythmodan treatment in female patients, resulting in Hypoglycaemia side effect. The patient was hospitalized.
Rythmodan Side Effect Report#5083861-5
Hypoglycaemia, Renal Disorder
This report suggests a potential Rythmodan Hypoglycaemia side effect(s) that can have serious consequences. A 53-year-old female patient (weight: NA) from Japan was diagnosed with the following symptoms/conditions: supraventricular tachycardia,iron deficiency,azotaemia,hypertension and used Rythmodan (dosage: NA) starting
Nov 01, 2000. After starting Rythmodan the patient began experiencing various side effects, including: Hypoglycaemia, Renal DisorderAdditional drugs used concurrently:
  • Ferromia
  • Kremezin
  • Cardenalin
  • Adalat
  • Depas
  • Cozaar
  • Calcium Carbonate
  • Bufferin
The patient was hospitalized. Although Rythmodan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hypoglycaemia, may still occur.
Rythmodan Side Effect Report#5042725-3
Dehydration, Hypoglycaemia, Hypoglycaemic Coma, Hypovolaemia, Pneumonia Aspiration, Renal Impairment
This Dehydration problem was reported by a physician from Japan. A 93-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertrophic cardiomyopathy,oedema peripheral. On
Mar 16, 2006 this consumer started treatment with Rythmodan (dosage: NA). The following drugs were being taken at the same time:
  • Lasix
  • Aldactone
  • Frandol
  • Sodium Bicarbonate
  • Gaster
  • Solanax
  • Magnesium Oxide
When using Rythmodan, the patient experienced the following unwanted symptoms/side effects: Dehydration, Hypoglycaemia, Hypoglycaemic Coma, Hypovolaemia, Pneumonia Aspiration, Renal ImpairmentAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dehydration, may become evident only after a product is in use by the general population.
Rythmodan Side Effect Report#5026543-8
Condition Aggravated, Dehydration, Hypoglycaemia, Hypoglycaemic Coma, Pneumonia Aspiration, Renal Impairment
This Condition Aggravated side effect was reported by a physician from Japan. A 93-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertrophic cardiomyopathy,oedema peripheral.The patient was prescribed Rythmodan (drug dosage: NA), which was initiated on
Mar 16, 2006. Concurrently used drugs:
  • Lasix
  • Aldactone
  • Frandol
  • Sodium Bicarbonate
  • Gaster
  • Solanax
  • Magnesium Oxide
.After starting to take Rythmodan the consumer reported adverse symptoms, such as: Condition Aggravated, Dehydration, Hypoglycaemia, Hypoglycaemic Coma, Pneumonia Aspiration, Renal ImpairmentThese side effects may potentially be related to Rythmodan.



The appearance of Rythmodan 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.

What are common Rythmodan Side Effects for Men?

Men Side EffectsReports

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.

    Rythmodan 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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    Rythmodan Safety Alerts, Active Ingredients, Usage Information

    More About Rythmodan

    Side Effects reported to FDA: 8

    Rythmodan safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 4

    Latest Rythmodan clinical trials