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SOLUPRED

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Solupred Adverse Events Reported to the FDA Over Time

How are Solupred adverse event reports trending over time?

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

Most Common Solupred Adverse Events Reported to the FDA

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

Diarrhoea
27 (1.48%)
Anaemia
26 (1.43%)
Toxic Skin Eruption
23 (1.26%)
Cytolytic Hepatitis
22 (1.21%)
Pyrexia
21 (1.15%)
Neutropenia
20 (1.1%)
Vomiting
18 (.99%)
Abdominal Pain
17 (.93%)
Drug Interaction
16 (.88%)
Inflammation
16 (.88%)
Purpura
15 (.82%)
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Renal Failure Acute
15 (.82%)
Tremor
15 (.82%)
Erythema
14 (.77%)
International Normalised Ratio Incr...
14 (.77%)
Lung Disorder
14 (.77%)
Malaise
14 (.77%)
Thrombocytopenia
14 (.77%)
Memory Impairment
13 (.71%)
Condition Aggravated
11 (.6%)
Dyspnoea
11 (.6%)
Nausea
11 (.6%)
Oedema Peripheral
11 (.6%)
Pruritus
11 (.6%)
Rash
11 (.6%)
Rash Erythematous
11 (.6%)
Alanine Aminotransferase Increased
10 (.55%)
Arthralgia
10 (.55%)
Aspartate Aminotransferase Increase...
10 (.55%)
Cholestasis
10 (.55%)
Pancreatitis Acute
10 (.55%)
Asthenia
9 (.49%)
Haematoma
9 (.49%)
Osteonecrosis
9 (.49%)
Rash Macular
9 (.49%)
Sepsis
9 (.49%)
Transplant Rejection
9 (.49%)
Arthritis
8 (.44%)
Blood Creatinine Increased
8 (.44%)
Confusional State
8 (.44%)
Cytomegalovirus Infection
8 (.44%)
Disorientation
8 (.44%)
Drug Ineffective
8 (.44%)
Rash Maculo-papular
8 (.44%)
Skin Lesion
8 (.44%)
Agranulocytosis
7 (.38%)
Cardio-respiratory Arrest
7 (.38%)
Convulsion
7 (.38%)
Cough
7 (.38%)
Deep Vein Thrombosis
7 (.38%)
Dysarthria
7 (.38%)
Fatigue
7 (.38%)
Hallucination, Auditory
7 (.38%)
Hepatitis
7 (.38%)
Hepatitis Cholestatic
7 (.38%)
Hypokalaemia
7 (.38%)
Jaundice
7 (.38%)
Lymphopenia
7 (.38%)
Nephrotic Syndrome
7 (.38%)
Nervous System Disorder
7 (.38%)
Pancreatitis
7 (.38%)
Somnolence
7 (.38%)
Stevens-johnson Syndrome
7 (.38%)
Subdural Haematoma
7 (.38%)
Acute Generalised Exanthematous Pus...
6 (.33%)
Cerebellar Syndrome
6 (.33%)
Cerebral Haemorrhage
6 (.33%)
Chromaturia
6 (.33%)
Coma
6 (.33%)
Dermatitis Bullous
6 (.33%)
Drug Exposure During Pregnancy
6 (.33%)
Eosinophilia
6 (.33%)
Fall
6 (.33%)
Gamma-glutamyltransferase Increased
6 (.33%)
Gastrointestinal Disorder
6 (.33%)
Grand Mal Convulsion
6 (.33%)
Haemorrhage
6 (.33%)
Hyperglycaemia
6 (.33%)
Hyperthermia
6 (.33%)
Hyperuricaemia
6 (.33%)
Insomnia
6 (.33%)
Leukopenia
6 (.33%)
Lipase Increased
6 (.33%)
Malignant Neoplasm Progression
6 (.33%)
Overdose
6 (.33%)
Platelet Count Decreased
6 (.33%)
Renal Failure
6 (.33%)
Renal Vein Thrombosis
6 (.33%)
Skin Exfoliation
6 (.33%)
Vasculitis
6 (.33%)
Abdominal Pain Upper
5 (.27%)
Acute Respiratory Failure
5 (.27%)
Colitis Ischaemic
5 (.27%)
Diabetes Mellitus
5 (.27%)
Diabetes Mellitus Inadequate Contro...
5 (.27%)
Febrile Neutropenia
5 (.27%)
Gait Disturbance
5 (.27%)
Headache
5 (.27%)
Hypoalbuminaemia
5 (.27%)
Hypotension
5 (.27%)
Interstitial Lung Disease
5 (.27%)

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

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

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

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

Drug Use For Unknown Indication
130
Product Used For Unknown Indication
43
Sinusitis
37
Renal Transplant
33
Crohns Disease
32
Bronchitis
24
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Prophylaxis
23
Premedication
21
Rheumatoid Arthritis
17
Prophylaxis Against Transplant Reje...
16
Multiple Myeloma
15
Pain
14
Asthma
12
Chemotherapy
9
Cough
7
B-cell Lymphoma
7
Chronic Obstructive Pulmonary Disea...
7
Colitis Ulcerative
7
Unevaluable Event
7
Dyspnoea
7
Heart Transplant
7
Lung Infection
5
General Physical Health Deteriorati...
5
Asthmatic Crisis
5
Infection
5
Brain Oedema
5
Toothache
5
Chest Pain
4
Pharyngitis
4
Lymphangiosis Carcinomatosa
4
Productive Cough
4
Diffuse Large B-cell Lymphoma
4
Hypersensitivity
3
Fatigue
3
Microscopic Polyangiitis
3
Bronchitis Chronic
3
Systemic Lupus Erythematosus
3
Anaemia
3
Neuralgia
3
Nasopharyngitis
3
Proctocolitis
3
Bronchial Disorder
3
Hodgkins Disease
3
Hypothyroidism
3
Tendonitis
3
Drug Exposure During Pregnancy
3
Behcets Syndrome
3
Rash
2
Bronchopneumopathy
2
Non-small Cell Lung Cancer
2
Acute Sinusitis
2

Solupred Case Reports

What Solupred 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 Solupred. 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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