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Moxonidine Side Effects

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Common Moxonidine Side Effects


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

Blood Creatinine Increased (9)
Asthenia (5)
Blood Iron Increased (4)
Blood Cholinesterase Decreased (4)
Blood Bilirubin Increased (4)
Aspartate Aminotransferase Increased (4)
Pneumonia (3)
Renal Failure (3)
Renal Failure Acute (2)
Nausea (2)
Somnolence (2)
Tremor (2)
Myocardial Infarction (2)
Vision Blurred (2)
Fatigue (2)
Electrocardiogram Qrs Complex Prolonged (2)
Haemoglobin Decreased (2)
Hyperkalaemia (2)
Hypertension (2)
Loss Of Consciousness (2)

➢ 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.

Moxonidine Side Effects Reported to FDA



Moxonidine Side Effect Report#9302557
Tremor, Balance Disorder, Mobility Decreased
This is a report of a 84-year-old female patient (weight: NA) from GB, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (moxonidine) (dosage: NA, start time:
Apr 12, 2013), combined with:
  • Paracetamol (paracetamol)
  • Salbutamol (salbutamol)
  • Seretide (seretide)
  • Tiotropium (tiotropium)
  • Warfarin (warfarin)
  • Sertraline (sertraline) (sertraline)
  • Bisoprolol (bisoprolol)
  • Digoxin (digoxin)
and developed a serious reaction and side effect(s): Tremor, Balance Disorder, Mobility Decreased after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine (moxonidine) treatment in female patients, resulting in Tremor side effect. The patient was hospitalized.
Moxonidine Side Effect Report#8477824-7
Gastric Ulcer Haemorrhage, Melaena, Haemoglobin Decreased, Anaemia
This report suggests a potential Moxonidine Gastric Ulcer Haemorrhage side effect(s) that can have serious consequences. A 89-year-old female patient (weight: NA) from United Kingdom was diagnosed with the following symptoms/conditions: NA and used Moxonidine (dosage: NA) starting
May 01, 2012. After starting Moxonidine the patient began experiencing various side effects, including: Gastric Ulcer Haemorrhage, Melaena, Haemoglobin Decreased, AnaemiaAdditional drugs used concurrently:
  • Amlodipine
  • Co-amilofruse
  • Ibuprofen (Unk)
  • Doxazosin
The patient was hospitalized. Although Moxonidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Gastric Ulcer Haemorrhage, may still occur.
Moxonidine Side Effect Report#8449894-3
Staphylococcal Sepsis, Complications Of Transplanted Kidney, Graft Haemorrhage, Renal Aneurysm
This Staphylococcal Sepsis problem was reported by a physician from Germany. A 48-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension,nephrogenic anaemia,infection prophylaxis,polyuria,prophylaxis against transplant rejection. On
Jan 02, 2011 this consumer started treatment with Moxonidine (dosage: 0.4 Mg, Bid). The following drugs were being taken at the same time:
  • Aranesp (40 Ug, Once Per Week)
  • Valcyte (450 Mg, On Monday And On Thursday)
  • Furosemide (80 Mg, Qd)
  • Mycophenolic Acid (1440 Mg, Unk)
  • Prednisone Tab (85 Mg, Unk)
  • Sandimmune (550 Mg, Unk)
  • Metoprolol Tartrate (95 Mg, Bid)
  • Fosamax (70 Mg, Once Weekly)
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: Staphylococcal Sepsis, Complications Of Transplanted Kidney, Graft Haemorrhage, Renal AneurysmThe 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 Staphylococcal Sepsis, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#8403159-4
Vision Blurred, Atrioventricular Block First Degree, Bundle Branch Block Right, Bradyarrhythmia, Asthenia, Dizziness, Electrocardiogram Repolarisation Abnormality, Electrocardiogram Qrs Complex Prolonged, Vertigo
This Vision Blurred side effect was reported by a health professional from Czech Republic. A 22-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Moxonidine (drug dosage: 0.4 Mg), which was initiated on NS. Concurrently used drugs:
  • Bisoprolol Fumarate (5 Mg Once Daily)
  • Verapamil/trandolapril (240 Mg/4 Mg)
.After starting to take Moxonidine the consumer reported adverse symptoms, such as: Vision Blurred, Atrioventricular Block First Degree, Bundle Branch Block Right, Bradyarrhythmia, Asthenia, Dizziness, Electrocardiogram Repolarisation Abnormality, Electrocardiogram Qrs Complex Prolonged, VertigoThese side effects may potentially be related to Moxonidine. The patient was hospitalized.
Moxonidine Side Effect Report#8402670-X
Fatigue, Abdominal Pain, Pneumonia, Constipation, Asthenia, Sepsis
This is a report of a female patient (weight: NA) from United States, suffering from the following health symptoms/conditions: hypertension,abdominal pain, who was treated with Moxonidine (dosage: 0.4 Mg, Unk, start time:
Feb 01, 2012), combined with:
  • Spasmomen (40 Mg, Bid)
  • Acetaminophen (1 G, Tid)
  • Amlogal (5 Mg, Unk)
  • Gemcitabine Hydrochloride (1000 Mg/m2, Unk)
  • Diamicron (60 Mg, Bid)
and developed a serious reaction and side effect(s): Fatigue, Abdominal Pain, Pneumonia, Constipation, Asthenia, Sepsis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine treatment in female patients, resulting in Fatigue side effect. The patient was hospitalized.
Moxonidine Side Effect Report#8351372-7
Chest Pain, Decreased Appetite, Asthenia, Dyspnoea Exertional, Blood Creatinine Increased, Nausea, Renal Failure Chronic
This report suggests a potential Moxonidine Chest Pain side effect(s) that can have serious consequences. A male patient (weight: NA) from Romania was diagnosed with the following symptoms/conditions: hypertension,myocardial ischaemia and used Moxonidine (dosage: NA) starting
Nov 19, 2011. After starting Moxonidine the patient began experiencing various side effects, including: Chest Pain, Decreased Appetite, Asthenia, Dyspnoea Exertional, Blood Creatinine Increased, Nausea, Renal Failure ChronicAdditional drugs used concurrently:
  • Isosorbide Dinitrate
  • Zemplar
  • Amlodipine Besylate
  • Zemplar
  • Allopurinol
  • Nitroglycerin
The patient was hospitalized. Although Moxonidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Chest Pain, may still occur.
Moxonidine Side Effect Report#8349234-4
Coronary Artery Disease, Angina Pectoris, Dyspnoea, Electrocardiogram Qrs Complex Prolonged, Atrial Fibrillation, Cardiac Failure, Blood Pressure Diastolic Decreased, Left Ventricular Hypertrophy, Blood Potassium Increased
This Coronary Artery Disease problem was reported by a physician from Germany. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Sep 30, 2003 this consumer started treatment with Moxonidine (dosage: 0.5 Mg/d). The following drugs were being taken at the same time:
  • Diuretics
  • Aldosterone Antagonists
  • Digoxin (0.2 Mg/d)
  • Pantoprazole (80 Mg/d)
  • Oral Antidiabetics
  • Insulin (36 Iu/d)
  • Marcumar (1.5 Mg/d)
  • Candesartan Cilexetil (16 Mg/d)
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: Coronary Artery Disease, Angina Pectoris, Dyspnoea, Electrocardiogram Qrs Complex Prolonged, Atrial Fibrillation, Cardiac Failure, Blood Pressure Diastolic Decreased, Left Ventricular Hypertrophy, Blood Potassium IncreasedThe 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 Coronary Artery Disease, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#8335323-7
Dizziness, Bradyarrhythmia, Sinus Arrest, Vision Blurred, Asthenia, Hypertension, Loss Of Consciousness
This Dizziness side effect was reported by a physician from Czech Republic. A 22-year-old male patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Moxonidine (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Bisoprolol Fumarate
  • Trandolapril And Verapamil Hydrochloride (Df = 240mg Verapamil/4mg Trandolapril)
.After starting to take Moxonidine the consumer reported adverse symptoms, such as: Dizziness, Bradyarrhythmia, Sinus Arrest, Vision Blurred, Asthenia, Hypertension, Loss Of ConsciousnessThese side effects may potentially be related to Moxonidine. The patient was hospitalized.
Moxonidine Side Effect Report#8330128-5
Tremor, Lethargy, Palpitations, Fatigue
This is a report of a 66-year-old male patient (weight: NA) from United Kingdom, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (dosage: NA, start time:
Jan 03, 2012), combined with:
  • Irbesartan
  • Topiramate
  • Levothyroxine Sodium
  • Diazepam
  • Bendroflumethiazide
  • Amlodipine Besylate
  • Dihydrocodeine Bitartrate Inj
  • Perindopril Erbumine
and developed a serious reaction and side effect(s): Tremor, Lethargy, Palpitations, Fatigue after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine treatment in male patients, resulting in Tremor side effect.
Moxonidine Side Effect Report#8297876-7
Acute Coronary Syndrome, C-reactive Protein Increased, Dilatation Atrial, Pneumonia, Muscular Weakness, Troponin Increased, Mitral Valve Disease, Gait Disturbance, Acute Myocardial Infarction
This report suggests a potential Moxonidine Acute Coronary Syndrome side effect(s) that can have serious consequences. A 47-year-old male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: hypertension and used Moxonidine (dosage: 0.4 Mg Daily) starting
Apr 01, 1999. After starting Moxonidine the patient began experiencing various side effects, including: Acute Coronary Syndrome, C-reactive Protein Increased, Dilatation Atrial, Pneumonia, Muscular Weakness, Troponin Increased, Mitral Valve Disease, Gait Disturbance, Acute Myocardial InfarctionAdditional drugs used concurrently:
  • Metoprolol Tartrate (95 Mg, Daily)
  • Ramipril (2.5 Mg, Unk)
  • Gilenya (0.5 Mg, Qd)
  • Clopidogrel (75 Mg, Unk)
  • Mictonorm (45 Mg, Daily)
  • Lioresal (35 Mg, Daily)
The patient was hospitalized. Although Moxonidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Acute Coronary Syndrome, may still occur.
Moxonidine Side Effect Report#8216353-2
Blood Pressure Diastolic Decreased, Blood Triglycerides Increased, Myocardial Infarction, Angina Pectoris
This Blood Pressure Diastolic Decreased problem was reported by a physician from Germany. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Jan 01, 2010 this consumer started treatment with Moxonidine (dosage: 0.6 Mg). The following drugs were being taken at the same time:
  • Rasilez Hct (1 Df, (150 Mg Alisk And 25 Mg Hydro) Daily)
  • Metformin Hydrochloride (2000 Mg, Per Day)
  • Alpha-adrenoceptor Blocking Agents
  • Hmg Coa Reductase Inhibitors (statins)
  • Laf237 (100 Mg)
  • Pentaerythritol Tetranitrate (160 Mg, Per Day)
  • Rasilez Hct (1 Df, (300 Mg Alsik And 25mg Hydro0 Daily)
  • Exforge (1 Df(160 Mg Vals And 10 Mg Hydro( Daily)
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: Blood Pressure Diastolic Decreased, Blood Triglycerides Increased, Myocardial Infarction, Angina PectorisThe 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 Pressure Diastolic Decreased, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#8112123-4
Hypokalaemia, Blood Urea Increased, Dehydration, Acute Prerenal Failure, Alkalosis, Blood Creatinine Increased, Hyponatraemia, Nausea, Constipation
This Hypokalaemia side effect was reported by a consumer or non-health professional from Germany. A 82-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Moxonidine (drug dosage: 0.3 Mg, 2x/day), which was initiated on
Jul 01, 2009. Concurrently used drugs:
  • Allopurinol (Unk)
  • Dipyrone Tab (Unk)
  • Bisoprolol Fumarate (5 Mg, 2x/day)
  • Xipamide (20 Mg, 1x/day)
  • Acetylsalicylic Acid Srt (100 Mg, 1x/day)
  • Pantoprazole (Unk)
  • Metformin (Unk)
  • Torsemide (10 Mg, 1x/day)
.After starting to take Moxonidine the consumer reported adverse symptoms, such as: Hypokalaemia, Blood Urea Increased, Dehydration, Acute Prerenal Failure, Alkalosis, Blood Creatinine Increased, Hyponatraemia, Nausea, ConstipationThese side effects may potentially be related to Moxonidine. The patient was hospitalized.
Moxonidine Side Effect Report#8066513-9
Hallucination, Visual, Paraesthesia, Anxiety
This is a report of a 78-year-old female patient (weight: NA) from United Kingdom, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (dosage: 600 Ug, Per Day, start time:
Dec 22, 2011), combined with:
  • Hydroxocobalamin
  • Aliskiren (150 Mg, Unk)
  • Laxido
and developed a serious reaction and side effect(s): Hallucination, Visual, Paraesthesia, Anxiety after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine treatment in female patients, resulting in Hallucination, Visual side effect.
Moxonidine Side Effect Report#8020969-6
Hyperkalaemia, Renal Failure Acute
This report suggests a potential Moxonidine (moxonidine) Hyperkalaemia side effect(s) that can have serious consequences. A 73-year-old female patient (weight: NA) from was diagnosed with the following symptoms/conditions: NA and used Moxonidine (moxonidine) (dosage: NA) starting NS. After starting Moxonidine (moxonidine) the patient began experiencing various side effects, including: Hyperkalaemia, Renal Failure AcuteAdditional drugs used concurrently:
  • Simvastatin
  • Ramipril (10 Mg (10 Mg, 1 In 1 D), Oral)
  • Furosemide (40 Mg (40 Mg, 1 In 1 D), Oral)
  • Metformin Hcl (3 Gm (1 Gm, 3 In 1 D), Oral)
  • Quinine Sulfate
  • Aspirin (75 Mg (75 Mg, 1 In 1 D), Oral)
The patient was hospitalized. Although Moxonidine (moxonidine) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hyperkalaemia, may still occur.
Moxonidine Side Effect Report#7978951-0
Breast Cancer, Blood Creatinine Increased, Renal Failure
This Breast Cancer problem was reported by a physician from Germany. A 67-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2008 this consumer started treatment with Moxonidine (dosage: Unk). The following drugs were being taken at the same time:
  • Ezetimibe (Unk)
  • Ramipril (5 Mg, 1x/day)
  • Aliskiren (1 Df, 1x/day)
  • Oxycodone (Unk)
  • Mirtazapine (Unk)
  • Naloxone (Unk)
  • Carvedilol (Unk)
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: Breast Cancer, Blood Creatinine Increased, Renal FailureThe 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 Breast Cancer, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#7939626-7
Extraskeletal Ossification, Wound Infection
This Extraskeletal Ossification side effect was reported by a physician from Germany. A male patient (weight:NA) experienced the following symptoms/conditions: hypertension,nephropathy.The patient was prescribed Moxonidine (drug dosage: 0.4 Mg, Per Day), which was initiated on
Dec 06, 2010. Concurrently used drugs:
  • Prednisone Tab (20 Mg, Per Day)
  • Ramipril (10 Mg, Per Day)
  • Furosemide (250 Mg, Per Day)
  • Budenofalk (6 Mg, Per Day)
  • Dekristol (20000 Iu, Per Month)
  • Rasilez (150 Mg, Per Day)
  • Kalinor (Unk)
  • Bayotensin Akut (As Needed)
.After starting to take Moxonidine the consumer reported adverse symptoms, such as: Extraskeletal Ossification, Wound InfectionThese side effects may potentially be related to Moxonidine. The patient was hospitalized.
Moxonidine Side Effect Report#7930478-8
Supraventricular Tachycardia, Electrocardiogram Qt Prolonged
This is a report of a 73-year-old female patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (dosage: NA, start time:
Oct 27, 2011), combined with:
  • Diltiazem Hcl
  • Digitoxin Tab
  • Glimepiride
  • Phenprocoumon
  • Torsemide
  • Pantoprazole Sodium
  • Hydrochlorothiazide
  • Pravastatin
and developed a serious reaction and side effect(s): Supraventricular Tachycardia, Electrocardiogram Qt Prolonged after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine treatment in female patients, resulting in Supraventricular Tachycardia side effect. The patient was hospitalized.
Moxonidine Side Effect Report#7797082-6
Blood Calcium Decreased, Hypoglycaemia
This report suggests a potential Moxonidine Blood Calcium Decreased side effect(s) that can have serious consequences. A 48-year-old female patient (weight: NA) from United Kingdom was diagnosed with the following symptoms/conditions: NA and used Moxonidine (dosage: NA) starting
Jul 28, 2011. After starting Moxonidine the patient began experiencing various side effects, including: Blood Calcium Decreased, HypoglycaemiaAdditional drugs used concurrently:
  • Eprex
  • Ezetimibe
  • Diltiazem Hcl
  • Renagel (2 Df, Tid)
  • Furosemide
  • Fexofenadine Hcl
  • Alfacalcidol
  • Hepatitis B Vaccine
Although Moxonidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Calcium Decreased, may still occur.
Moxonidine Side Effect Report#7773326-1
Somnolence, Accidental Overdose, Renal Failure, Coma
This Somnolence problem was reported by a health professional from Germany. A 89-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Moxonidine (dosage: NA). The following drugs were being taken at the same time:
  • Simvastatin
  • Clonazepam
  • Aspirin
  • Hydrochlorothiazide
  • Carboplatin
  • Metoprolol Tartrate
  • Lisinopril
  • Baclofen
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: Somnolence, Accidental Overdose, Renal Failure, ComaThe 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 Somnolence, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#7723809-5
Blood Urea Increased, Pulmonary Arterial Wedge Pressure Decreased, Asthenia, Dysuria, Cardiomyopathy, Prothrombin Time Prolonged, Hyperglycaemia, Obesity, Urinary Tract Disorder
This Blood Urea Increased side effect was reported by a physician from Germany. A female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Moxonidine (drug dosage: Unk Ukn, Unk), which was initiated on
Dec 07, 2010. Concurrently used drugs:
  • Lyrica (1 Df, Bid)
  • Clonidine (300 Ug, Unk)
  • Angiotensin Converting Enzyme Blockers (Unk Ukn, Unk)
  • Marcumar (Unk Ukn, Unk)
  • Protaphane (Unk Ukn, Unk)
  • Heparin (1 Df, Bid)
  • Carmen (20 Mg, Unk)
  • Insuman Rapid (70 Iu, Unk)
.After starting to take Moxonidine the consumer reported adverse symptoms, such as: Blood Urea Increased, Pulmonary Arterial Wedge Pressure Decreased, Asthenia, Dysuria, Cardiomyopathy, Prothrombin Time Prolonged, Hyperglycaemia, Obesity, Urinary Tract DisorderThese side effects may potentially be related to Moxonidine. The patient was hospitalized.
Moxonidine Side Effect Report#7684252-0
This is a report of a 80-year-old female patient (weight: NA) from United Kingdom, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (dosage: Unk, start time:
Oct 03, 2004), combined with:
  • Diltiazem (Unk)
  • Urapidil (Unk)
  • Ramipril (Unk)
  • Irbesartan (Unk)
  • Darbepoetin Alfa (38 Unit, Q2wk)
  • Aspirin (Unk)
  • Furosemide (Unk)
and developed a serious reaction and side effect(s): after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine treatment in female patients, resulting in Death side effect.
Moxonidine Side Effect Report#7587581-4
Myocardial Infarction, Blood Pressure Increased
This report suggests a potential Moxonidine Myocardial Infarction side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: hypertension and used Moxonidine (dosage: 0.2 Mg Per Day) starting
May 13, 2008. After starting Moxonidine the patient began experiencing various side effects, including: Myocardial Infarction, Blood Pressure IncreasedAdditional drugs used concurrently:
  • Statins
  • Metoprolol Tartrate (47.5 Mg Per Day)
Although Moxonidine demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Myocardial Infarction, may still occur.
Moxonidine Side Effect Report#7537622-5
Pneumonia
This Pneumonia problem was reported by a physician from Germany. A male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Nov 13, 2006 this consumer started treatment with Moxonidine (dosage: 0.6 Mg / Day). The following drugs were being taken at the same time:
  • Diovan (1 Df, Bid)
  • Diovan (1 Df, Qd)
  • Torsemide (20 Mg / Day)
  • Amlodipine (10 Mg/ Day)
When using Moxonidine, the patient experienced the following unwanted symptoms/side effects: PneumoniaThe 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 Pneumonia, may become evident only after a product is in use by the general population.
Moxonidine Side Effect Report#7460876-0
Faecaloma, Subileus
This Faecaloma side effect was reported by a pharmacist from Germany. A 89-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Moxonidine 0,3mg (drug dosage: .3 Milligram;), which was initiated on
Jan 01, 1999. Concurrently used drugs:
  • Amlodipine (10 Milligram;)
  • Metamizol (2250 Milligram;)
  • Bisoprolol 5mg (5 Milligram;)
  • Mictonorm 15mg (30 Milligram;)
  • Mirtazapin 15mg (7.5 Milligram;)
  • Acetylsalicylic Acid Srt (100 Milligram;)
  • Oxycodone 20mg (40 Milligram;)
  • Dekristol 20000 I.e. (1333.3333 Iu (international Unit);)
.After starting to take Moxonidine 0,3mg the consumer reported adverse symptoms, such as: Faecaloma, SubileusThese side effects may potentially be related to Moxonidine 0,3mg. The patient was hospitalized.
Moxonidine Side Effect Report#7436607-7
Withdrawal Syndrome
This is a report of a 65-year-old female patient (weight: NA) from United Kingdom, suffering from the following health symptoms/conditions: NA, who was treated with Moxonidine (moxonidine) (moxonidine) (dosage: NA, start time:
Nov 15, 2010), combined with:
  • Rosuvastatin
  • Bendrofluazide (bendrofluazide) (bendrofluazide)
  • Ropinirole (Oral Use)
and developed a serious reaction and side effect(s): Withdrawal Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Moxonidine (moxonidine) (moxonidine) treatment in female patients, resulting in Withdrawal Syndrome side effect.


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The appearance of Moxonidine 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.

    Moxonidine 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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    Moxonidine Safety Alerts, Active Ingredients, Usage Information

    More About Moxonidine

    Side Effects reported to FDA: 35

    Moxonidine safety alerts: No

    Reported deaths: 3

    Reported hospitalizations: 24

    Latest Moxonidine clinical trials