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MAGNESIUM SULFATE

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Magnesium Sulfate Adverse Events Reported to the FDA Over Time

How are Magnesium Sulfate adverse event reports trending over time?

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

Most Common Magnesium Sulfate Adverse Events Reported to the FDA

What are the most common Magnesium Sulfate adverse events reported to the FDA?

Drug Exposure During Pregnancy
95 (5.87%)
Medication Error
46 (2.84%)
Caesarean Section
25 (1.54%)
Hypocalcaemia
24 (1.48%)
Tachycardia Foetal
24 (1.48%)
Premature Baby
23 (1.42%)
Drug Ineffective
22 (1.36%)
Foetal Distress Syndrome
21 (1.3%)
Drug Interaction
20 (1.24%)
Hypermagnesaemia
20 (1.24%)
Hypotension
19 (1.17%)
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Blood Magnesium Increased
15 (.93%)
Maternal Drugs Affecting Foetus
15 (.93%)
Neonatal Disorder
15 (.93%)
Osteopenia
15 (.93%)
Dyspnoea
14 (.86%)
Malaise
14 (.86%)
Blood Alkaline Phosphatase Increase...
13 (.8%)
Toxic Epidermal Necrolysis
13 (.8%)
Cardiac Arrest
12 (.74%)
Nausea
12 (.74%)
Respiratory Failure
12 (.74%)
Drug Dispensing Error
11 (.68%)
Incorrect Dose Administered
11 (.68%)
Neuromuscular Blockade
11 (.68%)
Oxygen Saturation Decreased
11 (.68%)
Apgar Score Low
9 (.56%)
Condition Aggravated
9 (.56%)
Grand Mal Convulsion
9 (.56%)
Pre-eclampsia
9 (.56%)
Vomiting
9 (.56%)
Convulsion
8 (.49%)
Depressed Level Of Consciousness
8 (.49%)
Drug Exposure Via Breast Milk
8 (.49%)
Drug Toxicity
8 (.49%)
Infusion Related Reaction
8 (.49%)
Pulmonary Oedema
8 (.49%)
Somnolence
8 (.49%)
Unresponsive To Stimuli
8 (.49%)
Accidental Overdose
7 (.43%)
Asthma
7 (.43%)
Blood Glucose Increased
7 (.43%)
Blood Pressure Decreased
7 (.43%)
Blood Pressure Increased
7 (.43%)
Chest Discomfort
7 (.43%)
Coma
7 (.43%)
Diarrhoea
7 (.43%)
Hypertension
7 (.43%)
Loss Of Consciousness
7 (.43%)
Neuromuscular Block Prolonged
7 (.43%)
Pneumonia
7 (.43%)
Tremor
7 (.43%)
Apallic Syndrome
6 (.37%)
Blood Calcium Decreased
6 (.37%)
Bradycardia
6 (.37%)
Cerebrovascular Disorder
6 (.37%)
Circumstance Or Information Capable...
6 (.37%)
Completed Suicide
6 (.37%)
Death
6 (.37%)
Dizziness
6 (.37%)
Hyperhidrosis
6 (.37%)
Overdose
6 (.37%)
Premature Labour
6 (.37%)
Procedural Hypotension
6 (.37%)
Pulmonary Interstitial Emphysema Sy...
6 (.37%)
Pyrexia
6 (.37%)
Renal Impairment
6 (.37%)
Rib Fracture
6 (.37%)
Urticaria
6 (.37%)
Ventricular Tachycardia
6 (.37%)
Asthenia
5 (.31%)
Chest Pain
5 (.31%)
Disseminated Intravascular Coagulat...
5 (.31%)
Feeling Hot
5 (.31%)
Flushing
5 (.31%)
Heart Rate Increased
5 (.31%)
Intra-uterine Death
5 (.31%)
Multi-organ Failure
5 (.31%)
Muscle Spasms
5 (.31%)
Neonatal Respiratory Distress Syndr...
5 (.31%)
Respiratory Arrest
5 (.31%)
Respiratory Depression
5 (.31%)
Respiratory Distress
5 (.31%)
Respiratory Rate Decreased
5 (.31%)
Urine Output Decreased
5 (.31%)
Wrong Drug Administered
5 (.31%)
Anaemia
4 (.25%)
Cardiovascular Disorder
4 (.25%)
Congenital Anomaly
4 (.25%)
Congenital Musculoskeletal Anomaly
4 (.25%)
Craniotabes
4 (.25%)
Drug Administration Error
4 (.25%)
Dysarthria
4 (.25%)
Electrocardiogram Qt Prolonged
4 (.25%)
Encephalopathy
4 (.25%)
Fatigue
4 (.25%)
Gait Disturbance
4 (.25%)
Headache
4 (.25%)
Hepatic Enzyme Increased
4 (.25%)
Hypersensitivity
4 (.25%)
Hypotonia Neonatal
4 (.25%)

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

What are the most common Magnesium Sulfate adverse events reported to the FDA?

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

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

Drug Use For Unknown Indication
323
Product Used For Unknown Indication
304
Constipation
209
Prophylaxis
132
Hypomagnesaemia
120
Mineral Supplementation
51
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Premedication
44
Pre-eclampsia
29
Asthma
27
Supplementation Therapy
26
Blood Magnesium Decreased
23
Electrolyte Substitution Therapy
21
Constipation Prophylaxis
21
Medical Diet
18
Drug Exposure During Pregnancy
18
Premature Labour
18
Tocolysis
18
Muscle Spasms
16
Ventricular Tachycardia
15
Magnesium Deficiency
13
Vitamin Supplementation
12
Eclampsia
11
Ill-defined Disorder
8
Routine Health Maintenance
8
Status Asthmaticus
7
Spinal Anaesthesia
7
Cardiac Failure Congestive
6
Nutritional Support
5
Myalgia
5
Parenteral Nutrition
5
Electrolyte Imbalance
5
Arrhythmia
4
Blood Magnesium
4
Adverse Drug Reaction
4
Dialysis
4
Palmar-plantar Erythrodysaesthesia ...
4
Torsade De Pointes
4
Hypertension
4
Convulsion Prophylaxis
4
Guillain-barre Syndrome
3
Hypoxia
3
Laxative Supportive Care
3
Substitution Therapy
3
Intensive Care
3
Convulsion
3
Bronchospasm
3
Myocardial Ischaemia
3
Migraine
3
Colon Cancer
3
Gastrointestinal Disorder
3
Respiratory Distress
3

Drug Labels

LabelLabelerEffective
Magnesium SulfateHospira, Inc.27-MAY-10
Pepsom Sports Spearmint The Pepsom Group, Inc.27-MAY-10
Magnesium SulfatePhysicians Total Care, Inc.27-MAY-10
Pepsom Sports Wintergreen The Pepsom Group, Inc.27-MAY-10
Pepsom Salt Peppermint The Pepsom Group, Inc.27-MAY-10
Magnesium SulfateGeneral Injectables & Vaccines, Inc24-AUG-10
Magnesium SulfateGeneral Injectables & Vaccines, Inc09-SEP-10
Magnesium SulfateGeneral Injectables & Vaccines, Inc06-JUN-11
Magnesium SulfateAPP Pharmaceuticals, LLC23-JUN-11
Magnesium SulfateAmerican Regent, Inc.22-DEC-11
Magnesium SulfateHospira, Inc.06-MAR-12
Magnesium Sulfate In DextroseHospira, Inc.06-MAR-12
Epsom Saltsoaking SolutionAdvanced Beauty Systems, Inc.20-JUN-12
Magnesium SulfateFresenius Kabi USA, LLC13-SEP-12
Suprep Bowel PrepBraintree Laboratories, Inc.06-NOV-12
Magnesium SulfateCantrell Drug Company21-NOV-12
Magnesium SulfateCantrell Drug Company21-NOV-12
SuclearBraintree Laboratories, Inc.31-JAN-13
Magnesium SulfateCardinal Health08-MAR-13
Magnesium SulfateHospira, Inc.10-APR-13

Magnesium Sulfate Case Reports

What Magnesium Sulfate 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 Magnesium Sulfate. 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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