DrugCite
Search

ALDOMET

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Aldomet Adverse Events Reported to the FDA Over Time

How are Aldomet adverse event reports trending over time?

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

Most Common Aldomet Adverse Events Reported to the FDA

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

Drug Exposure During Pregnancy
126 (7.71%)
Caesarean Section
40 (2.45%)
Premature Baby
37 (2.26%)
Hypertension
23 (1.41%)
Pyrexia
21 (1.29%)
Blood Pressure Increased
20 (1.22%)
Foetal Growth Retardation
16 (.98%)
Headache
16 (.98%)
Haemolytic Anaemia
15 (.92%)
Oligohydramnios
15 (.92%)
Abortion Spontaneous
14 (.86%)
Show More Show More
Alanine Aminotransferase Increased
13 (.8%)
Foetal Arrhythmia
13 (.8%)
Pre-eclampsia
13 (.8%)
Pregnancy
13 (.8%)
Pulmonary Oedema
13 (.8%)
Abnormal Labour
12 (.73%)
Blood Pressure Inadequately Control...
12 (.73%)
Drug Ineffective
12 (.73%)
Hepatic Function Abnormal
12 (.73%)
Liver Disorder
12 (.73%)
Aspartate Aminotransferase Increase...
11 (.67%)
Dyspnoea
11 (.67%)
Neonatal Respiratory Distress Syndr...
11 (.67%)
Protein Urine Present
11 (.67%)
Proteinuria
11 (.67%)
Somnolence
11 (.67%)
Abortion Induced
10 (.61%)
Gamma-glutamyltransferase Increased
10 (.61%)
Hellp Syndrome
10 (.61%)
Patent Ductus Arteriosus
10 (.61%)
Renal Failure
10 (.61%)
Bronchopulmonary Dysplasia
9 (.55%)
Dizziness
9 (.55%)
Hypotension
9 (.55%)
Interstitial Lung Disease
9 (.55%)
Jaundice
9 (.55%)
Jaundice Neonatal
9 (.55%)
Pulmonary Arterial Hypertension
9 (.55%)
Breech Presentation
8 (.49%)
Chills
8 (.49%)
Eclampsia
8 (.49%)
Face Oedema
8 (.49%)
Glomerulonephritis Chronic
8 (.49%)
Maternal Drugs Affecting Foetus
8 (.49%)
Renal Aplasia
8 (.49%)
Renal Failure Acute
8 (.49%)
Ventricular Hypertrophy
8 (.49%)
Drug Rash With Eosinophilia And Sys...
7 (.43%)
Dysarthria
7 (.43%)
Hypotonia Neonatal
7 (.43%)
Nausea
7 (.43%)
Oedema Peripheral
7 (.43%)
Renal Impairment
7 (.43%)
Small For Dates Baby
7 (.43%)
Colitis Ulcerative
6 (.37%)
Congenital Anomaly
6 (.37%)
Congenital Cytomegalovirus Infectio...
6 (.37%)
Conjunctivitis
6 (.37%)
Depressed Level Of Consciousness
6 (.37%)
Hepatitis Acute
6 (.37%)
Hypospadias
6 (.37%)
Omphalitis
6 (.37%)
Parotitis
6 (.37%)
Rash
6 (.37%)
Rhabdomyolysis
6 (.37%)
Solitary Kidney
6 (.37%)
Staphylococcal Sepsis
6 (.37%)
Tachycardia
6 (.37%)
Umbilical Cord Abnormality
6 (.37%)
Anaemia
5 (.31%)
Cholelithiasis
5 (.31%)
Cough
5 (.31%)
Fatigue
5 (.31%)
Foetal Disorder
5 (.31%)
Foetal Distress Syndrome
5 (.31%)
Haemoglobin Decreased
5 (.31%)
Hepatitis
5 (.31%)
Hepatomegaly
5 (.31%)
Neonatal Disorder
5 (.31%)
Oedema
5 (.31%)
Overdose
5 (.31%)
Pancytopenia
5 (.31%)
Renal Tubular Disorder
5 (.31%)
Ventricular Septal Defect
5 (.31%)
Abdominal Distension
4 (.24%)
Abdominal Pain Upper
4 (.24%)
Akathisia
4 (.24%)
Atrial Fibrillation
4 (.24%)
Azotaemia
4 (.24%)
Blood Creatine Phosphokinase Increa...
4 (.24%)
Blood Pressure Fluctuation
4 (.24%)
Body Temperature Increased
4 (.24%)
C-reactive Protein Increased
4 (.24%)
Cerebral Haematoma
4 (.24%)
Condition Aggravated
4 (.24%)
Confusional State
4 (.24%)
Congenital Tricuspid Valve Atresia
4 (.24%)
Delayed Fontanelle Closure
4 (.24%)
Drug Effect Decreased
4 (.24%)
Drug Exposure Via Breast Milk
4 (.24%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Hypertension
371
Product Used For Unknown Indication
26
Pregnancy Induced Hypertension
20
Drug Use For Unknown Indication
19
Blood Pressure
18
Essential Hypertension
17
Show More Show More
Drug Exposure During Pregnancy
11
Maternal Exposure Timing Unspecifie...
4
Blood Pressure Increased
4
Blood Pressure Abnormal
4
Pre-eclampsia
3
Gestational Hypertension
2
Positron Emission Tomogram
2
Dementia
1
Hypertensive Nephropathy
1
Hypercalcaemia
1
Blood Pressure Management
1
Myocardial Ischaemia
1
Suicide Attempt
1
Hyperlipidaemia
1
Parkinsonism
1
Albumin Globulin Ratio Abnormal
1

Aldomet Case Reports

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

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Aldomet. 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.

Comments

Share your experience with Aldomet.