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Logimax Adverse Events Reported to the FDA Over Time

How are Logimax adverse event reports trending over time?

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

Most Common Logimax Adverse Events Reported to the FDA

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

Renal Failure Acute
9 (5.17%)
Generalised Oedema
6 (3.45%)
Malaise
6 (3.45%)
Nephrotic Syndrome
6 (3.45%)
Weight Increased
6 (3.45%)
Hypokalaemia
5 (2.87%)
Glomerulonephritis Membranous
4 (2.3%)
Hyperkeratosis
4 (2.3%)
Mycosis Fungoides
4 (2.3%)
Pruritus
4 (2.3%)
Biopsy Kidney Abnormal
3 (1.72%)
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Blood Albumin Decreased
3 (1.72%)
Bradycardia
3 (1.72%)
Drug Eruption
3 (1.72%)
Hyponatraemia
3 (1.72%)
Hypotension
3 (1.72%)
Lichenoid Keratosis
3 (1.72%)
Oedema Peripheral
3 (1.72%)
Protein Urine Present
3 (1.72%)
Rash Erythematous
3 (1.72%)
Rash Papular
3 (1.72%)
Blood Pressure Increased
2 (1.15%)
Depression
2 (1.15%)
Electrocardiogram Qt Prolonged
2 (1.15%)
Glomerulonephritis
2 (1.15%)
Haemorrhagic Fever
2 (1.15%)
Hepatitis
2 (1.15%)
Hepatitis Acute
2 (1.15%)
Hypertension
2 (1.15%)
Hypoalbuminaemia
2 (1.15%)
Hypothermia
2 (1.15%)
Morganella Infection
2 (1.15%)
Oedema
2 (1.15%)
Proteinuria
2 (1.15%)
Prurigo
2 (1.15%)
Renal Failure
2 (1.15%)
Rhabdomyolysis
2 (1.15%)
Septic Shock
2 (1.15%)
Thrombocytopenia
2 (1.15%)
Urticaria
2 (1.15%)
Agoraphobia
1 (.57%)
Alpha 2 Globulin Increased
1 (.57%)
Angiopathy
1 (.57%)
Anxiety
1 (.57%)
Asthenia
1 (.57%)
Beta Globulin Decreased
1 (.57%)
Blood Immunoglobulin M
1 (.57%)
Bone Marrow Failure
1 (.57%)
Bundle Branch Block
1 (.57%)
Cerebrovascular Accident
1 (.57%)
Cholestasis
1 (.57%)
Conduction Disorder
1 (.57%)
Confusional State
1 (.57%)
Deafness Unilateral
1 (.57%)
Decreased Appetite
1 (.57%)
Diarrhoea
1 (.57%)
Diarrhoea Infectious
1 (.57%)
Diverticular Perforation
1 (.57%)
Diverticulitis
1 (.57%)
Dizziness
1 (.57%)
Drug Ineffective
1 (.57%)
Drug Interaction
1 (.57%)
Dyslipidaemia
1 (.57%)
Dyspnoea Exertional
1 (.57%)
Electrocardiogram Repolarisation Ab...
1 (.57%)
Escherichia Infection
1 (.57%)
Escherichia Sepsis
1 (.57%)
Eye Disorder
1 (.57%)
Eyelid Oedema
1 (.57%)
Fall
1 (.57%)
Gait Disturbance
1 (.57%)
General Physical Health Deteriorati...
1 (.57%)
Hyperkalaemia
1 (.57%)
Hypochloraemia
1 (.57%)
Hypogammaglobulinaemia
1 (.57%)
Iatrogenic Injury
1 (.57%)
Lichenification
1 (.57%)
Myocardial Infarction
1 (.57%)
Oedema Genital
1 (.57%)
Pancytopenia
1 (.57%)
Sinus Bradycardia
1 (.57%)
Surgery
1 (.57%)
Tinnitus
1 (.57%)
Toxic Skin Eruption
1 (.57%)
Tremor
1 (.57%)
Urinary Incontinence
1 (.57%)
Ventricular Extrasystoles
1 (.57%)
Vertigo
1 (.57%)
Viral Infection
1 (.57%)

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This graph shows the top adverse events submitted to the FDA for Logimax, 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 Logimax 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 Logimax

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

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This graph shows the top categories of adverse events submitted to the FDA for Logimax, 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 Logimax 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 Logimax According to Those Reporting Adverse Events

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

Hypertension
40
Drug Use For Unknown Indication
13
Essential Hypertension
7
Product Used For Unknown Indication
4
Ill-defined Disorder
2
Hypercholesterolaemia
1
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Hypertonia
1

Logimax Case Reports

What Logimax 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 Logimax. 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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