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MOVIPREP

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Moviprep Adverse Events Reported to the FDA Over Time

How are Moviprep adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Moviprep, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Moviprep is flagged as the suspect drug causing the adverse event.

Most Common Moviprep Adverse Events Reported to the FDA

What are the most common Moviprep adverse events reported to the FDA?

Vomiting
40 (3.65%)
Dehydration
27 (2.46%)
Nausea
24 (2.19%)
Convulsion
19 (1.73%)
Hypokalaemia
17 (1.55%)
Diarrhoea
14 (1.28%)
Dyspnoea
14 (1.28%)
Fall
14 (1.28%)
Headache
14 (1.28%)
Dizziness
13 (1.19%)
Hyponatraemia
13 (1.19%)
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Blood Pressure Increased
12 (1.09%)
Urticaria
12 (1.09%)
Abdominal Pain
11 (1%)
Renal Failure Acute
11 (1%)
Abdominal Distension
10 (.91%)
Drug Hypersensitivity
10 (.91%)
Anaphylactic Shock
9 (.82%)
Atrial Fibrillation
9 (.82%)
Loss Of Consciousness
9 (.82%)
Muscle Spasms
9 (.82%)
Swelling Face
9 (.82%)
Syncope
9 (.82%)
Chills
8 (.73%)
Confusional State
8 (.73%)
Fatigue
8 (.73%)
Hypersensitivity
8 (.73%)
Malaise
8 (.73%)
Pain In Extremity
8 (.73%)
Tremor
8 (.73%)
Anaphylactic Reaction
7 (.64%)
Condition Aggravated
7 (.64%)
Erythema
7 (.64%)
Oedema Peripheral
7 (.64%)
Retching
7 (.64%)
White Blood Cell Count Increased
7 (.64%)
Electrolyte Imbalance
6 (.55%)
Eye Swelling
6 (.55%)
Flatulence
6 (.55%)
Pain
6 (.55%)
Pruritus
6 (.55%)
Blood Chloride Decreased
5 (.46%)
Colitis Ischaemic
5 (.46%)
Disorientation
5 (.46%)
Drug Ineffective
5 (.46%)
Dysgeusia
5 (.46%)
Dysphagia
5 (.46%)
Eructation
5 (.46%)
Gastrooesophageal Reflux Disease
5 (.46%)
Head Injury
5 (.46%)
Insomnia
5 (.46%)
Pallor
5 (.46%)
Paraesthesia
5 (.46%)
Rash
5 (.46%)
Swelling
5 (.46%)
Asthenia
4 (.36%)
Atrial Flutter
4 (.36%)
Blood Glucose Increased
4 (.36%)
Blood Magnesium Decreased
4 (.36%)
Blood Potassium Decreased
4 (.36%)
Bradycardia
4 (.36%)
Cardiac Arrest
4 (.36%)
Cerebral Haemorrhage
4 (.36%)
Chest Discomfort
4 (.36%)
Chest Pain
4 (.36%)
Colitis
4 (.36%)
Conjunctival Haemorrhage
4 (.36%)
Feeling Abnormal
4 (.36%)
Gastrointestinal Sounds Abnormal
4 (.36%)
General Physical Health Deteriorati...
4 (.36%)
Haemoglobin Decreased
4 (.36%)
Irritable Bowel Syndrome
4 (.36%)
Mean Platelet Volume Decreased
4 (.36%)
Presyncope
4 (.36%)
Pyrexia
4 (.36%)
Rash Maculo-papular
4 (.36%)
Swollen Tongue
4 (.36%)
Unresponsive To Stimuli
4 (.36%)
Abortion Spontaneous
3 (.27%)
Accidental Exposure
3 (.27%)
Aggression
3 (.27%)
Angioedema
3 (.27%)
Appendicitis
3 (.27%)
Arrhythmia
3 (.27%)
Blood Calcium Decreased
3 (.27%)
Blood Sodium Decreased
3 (.27%)
Cyanosis
3 (.27%)
Dialysis
3 (.27%)
Disturbance In Attention
3 (.27%)
Drug Effect Decreased
3 (.27%)
Drug Exposure During Pregnancy
3 (.27%)
Drug Interaction
3 (.27%)
Face Oedema
3 (.27%)
Faecal Incontinence
3 (.27%)
Frequent Bowel Movements
3 (.27%)
Gait Disturbance
3 (.27%)
Gout
3 (.27%)
Haematoma
3 (.27%)
Hearing Impaired
3 (.27%)
Hypotension
3 (.27%)
Hypotonia
3 (.27%)

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This graph shows the top adverse events submitted to the FDA for Moviprep, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Moviprep is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Moviprep

What are the most common Moviprep adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Moviprep, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Moviprep is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Moviprep According to Those Reporting Adverse Events

Why are people taking Moviprep, according to those reporting adverse events to the FDA?

Constipation
273
Colonoscopy
140
Product Used For Unknown Indication
97
Bowel Preparation
82
Prophylaxis
14
Constipation Prophylaxis
12
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Preoperative Care
11
Laxative Supportive Care
10
Gastritis Prophylaxis
4
Infrequent Bowel Movements
3
Ill-defined Disorder
2
Colitis Ulcerative
2
Crohns Disease
2
Gastritis
1
Hepatic Cancer Metastatic
1
Drug Abuse
1
Haematochezia
1
Gastrointestinal Motility Disorder
1
Drug Use For Unknown Indication
1

Drug Labels

LabelLabelerEffective
MoviprepPhysicians Total Care, Inc.30-NOV-09
MoviprepSalix Pharmaceuticals, Inc.20-MAR-13

Moviprep Case Reports

What Moviprep safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Moviprep. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

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