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MORPHINE SULFATE INJ

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Morphine Sulfate Inj Adverse Events Reported to the FDA Over Time

How are Morphine Sulfate Inj adverse event reports trending over time?

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

Most Common Morphine Sulfate Inj Adverse Events Reported to the FDA

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

Drug Interaction
32 (2.82%)
Hypotension
23 (2.03%)
Overdose
22 (1.94%)
Death
21 (1.85%)
Drug Toxicity
21 (1.85%)
Cardio-respiratory Arrest
19 (1.67%)
Respiratory Depression
15 (1.32%)
Unresponsive To Stimuli
15 (1.32%)
Sedation
14 (1.23%)
Somnolence
14 (1.23%)
Back Pain
12 (1.06%)
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Pain
12 (1.06%)
Drug Exposure During Pregnancy
11 (.97%)
Drug Withdrawal Syndrome
11 (.97%)
Therapeutic Agent Toxicity
11 (.97%)
Depressed Level Of Consciousness
10 (.88%)
Asthenia
9 (.79%)
Medication Error
9 (.79%)
Agitation
8 (.7%)
Drug Effect Decreased
8 (.7%)
Incorrect Dose Administered
8 (.7%)
Respiratory Failure
8 (.7%)
Vomiting
8 (.7%)
White Blood Cell Count Increased
8 (.7%)
Anaesthetic Complication
7 (.62%)
Areflexia
7 (.62%)
Confusional State
7 (.62%)
Delirium
7 (.62%)
Headache
7 (.62%)
Nausea
7 (.62%)
Post Procedural Complication
7 (.62%)
Apnoea
6 (.53%)
Cardiac Arrest
6 (.53%)
Haemoglobin Decreased
6 (.53%)
Hyperaesthesia
6 (.53%)
Infection
6 (.53%)
Lethargy
6 (.53%)
Myoclonus
6 (.53%)
Oxygen Saturation Decreased
6 (.53%)
Procedural Hypotension
6 (.53%)
Suicide Attempt
6 (.53%)
Accidental Overdose
5 (.44%)
Coma
5 (.44%)
Drug Abuse
5 (.44%)
Fatigue
5 (.44%)
Haemorrhage
5 (.44%)
Inadequate Analgesia
5 (.44%)
Insomnia
5 (.44%)
Malaise
5 (.44%)
Paraesthesia
5 (.44%)
Pleural Effusion
5 (.44%)
Pneumonia Aspiration
5 (.44%)
Pyrexia
5 (.44%)
Renal Impairment
5 (.44%)
Respiratory Distress
5 (.44%)
Respiratory Rate Decreased
5 (.44%)
Abdominal Pain
4 (.35%)
Acute Generalised Exanthematous Pus...
4 (.35%)
Aggression
4 (.35%)
Anxiety
4 (.35%)
Cognitive Disorder
4 (.35%)
Condition Aggravated
4 (.35%)
Disorientation
4 (.35%)
Drug Ineffective
4 (.35%)
Dysarthria
4 (.35%)
Dysphagia
4 (.35%)
Fistula
4 (.35%)
Granuloma
4 (.35%)
Hyperkalaemia
4 (.35%)
Hyperventilation
4 (.35%)
Hypoaesthesia
4 (.35%)
Irritability
4 (.35%)
Mental Status Changes
4 (.35%)
Myalgia
4 (.35%)
Obstetric Procedure Complication
4 (.35%)
Peritonitis
4 (.35%)
Post Procedural Haemorrhage
4 (.35%)
Pulmonary Oedema
4 (.35%)
Renal Failure Acute
4 (.35%)
Respiratory Arrest
4 (.35%)
Sensory Loss
4 (.35%)
Swelling
4 (.35%)
Urinary Retention
4 (.35%)
Abscess
3 (.26%)
Acute Abdomen
3 (.26%)
Altered State Of Consciousness
3 (.26%)
Amnesia
3 (.26%)
Ascites
3 (.26%)
Bacterial Infection
3 (.26%)
Blood Pressure Decreased
3 (.26%)
Blood Pressure Systolic Decreased
3 (.26%)
Bradycardia
3 (.26%)
Catheter Related Complication
3 (.26%)
Chest Pain
3 (.26%)
Cholecystitis
3 (.26%)
Depression
3 (.26%)
Device Failure
3 (.26%)
Diarrhoea
3 (.26%)
Disease Progression
3 (.26%)
Erythema
3 (.26%)
Fall
3 (.26%)

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

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

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

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

Pain
66
Drug Use For Unknown Indication
65
Product Used For Unknown Indication
27
Spinal Anaesthesia
25
Analgesic Effect
17
Analgesia
14
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Procedural Pain
14
Analgesic Therapy
13
Back Pain
13
Pain Management
12
Postoperative Analgesia
11
Cancer Pain
10
Abdominal Pain
7
Maintenance Of Anaesthesia
7
Musculoskeletal Pain
4
Premedication
4
Rheumatoid Arthritis
3
Epidural Anaesthesia
3
Pain In Extremity
3
Neuralgia
2
Sedative Therapy
2
Arthralgia
2
Surgery
2
Post Procedural Pain
2
Intentional Misuse
2
Myelitis Transverse
2
Pleuritic Pain
2
General Anaesthesia
1
Buttock Pain
1
Postoperative Care
1
Sciatica
1
Spinal Column Stenosis
1
Nausea
1
Back Disorder
1
Intentional Drug Misuse
1
Off Label Use
1
Neuropathy Peripheral
1
Metastatic Pain
1
Ligament Injury
1
Muscle Spasms
1
Ligament Rupture
1
Extubation
1
Breakthrough Pain
1
Anaesthesia
1
Suicide Attempt
1
Spinal Fusion Surgery
1
Drug Abuse
1
Medication Error
1

Morphine Sulfate Inj Case Reports

What Morphine Sulfate Inj 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 Morphine Sulfate Inj. 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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