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STEROIDS NOS

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Steroids Nos Adverse Events Reported to the FDA Over Time

How are Steroids Nos adverse event reports trending over time?

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

Most Common Steroids Nos Adverse Events Reported to the FDA

What are the most common Steroids Nos adverse events reported to the FDA?

Pyrexia
96 (1.91%)
Tendon Rupture
67 (1.34%)
Rotator Cuff Syndrome
60 (1.2%)
Blood Creatinine Increased
56 (1.12%)
Diarrhoea
38 (.76%)
Fatigue
38 (.76%)
Urinary Tract Infection
37 (.74%)
Abdominal Pain
36 (.72%)
Cytomegalovirus Infection
35 (.7%)
Headache
35 (.7%)
Acute Graft Versus Host Disease
31 (.62%)
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Convulsion
30 (.6%)
Dyspnoea
30 (.6%)
Infection
30 (.6%)
Nausea
30 (.6%)
Pain
30 (.6%)
Tendonitis
30 (.6%)
Alanine Aminotransferase Increased
27 (.54%)
Hypertension
27 (.54%)
Oedema Peripheral
26 (.52%)
Arthralgia
25 (.5%)
Epstein-barr Virus Infection
25 (.5%)
Anaemia
24 (.48%)
Drug Ineffective
24 (.48%)
Meniscus Lesion
24 (.48%)
Hepatic Function Abnormal
23 (.46%)
Joint Injury
23 (.46%)
Anxiety
22 (.44%)
Cataract
22 (.44%)
Cytomegalovirus Viraemia
22 (.44%)
Depression
22 (.44%)
Kidney Transplant Rejection
22 (.44%)
Surgery
22 (.44%)
Chronic Graft Versus Host Disease
21 (.42%)
Pneumatosis Intestinalis
21 (.42%)
Pneumonia
21 (.42%)
Sepsis
21 (.42%)
Vomiting
21 (.42%)
Lung Infiltration
20 (.4%)
Pain In Extremity
20 (.4%)
Cough
19 (.38%)
Pneumocystis Jiroveci Pneumonia
19 (.38%)
Staphylococcal Infection
19 (.38%)
Blood Beta-d-glucan Increased
18 (.36%)
Bursitis
18 (.36%)
Gait Disturbance
18 (.36%)
Muscle Spasms
18 (.36%)
Proteinuria
18 (.36%)
Renal Impairment
18 (.36%)
Death
17 (.34%)
Insomnia
17 (.34%)
Joint Swelling
17 (.34%)
Musculoskeletal Stiffness
17 (.34%)
Myalgia
17 (.34%)
Nephropathy Toxic
17 (.34%)
Tracheobronchitis
17 (.34%)
Tremor
17 (.34%)
Back Pain
16 (.32%)
Fall
16 (.32%)
Graft Versus Host Disease
16 (.32%)
Osteonecrosis
16 (.32%)
Dehydration
15 (.3%)
Diabetes Mellitus
15 (.3%)
Hypotension
15 (.3%)
Lymphadenopathy
15 (.3%)
Neutropenia
15 (.3%)
Thrombocytopenia
15 (.3%)
Focal Segmental Glomerulosclerosis
14 (.28%)
Gastrointestinal Haemorrhage
14 (.28%)
Interstitial Lung Disease
14 (.28%)
Osteoarthritis
14 (.28%)
Respiratory Failure
14 (.28%)
Tenosynovitis
14 (.28%)
Weight Increased
14 (.28%)
Asthma
13 (.26%)
Blood Glucose Increased
13 (.26%)
Hyperglycaemia
13 (.26%)
Multi-organ Failure
13 (.26%)
Muscle Rupture
13 (.26%)
Musculoskeletal Pain
13 (.26%)
Pseudomonas Infection
13 (.26%)
Renal Failure Acute
13 (.26%)
Agitation
12 (.24%)
Aspartate Aminotransferase Increase...
12 (.24%)
Epstein-barr Virus Associated Lymph...
12 (.24%)
Febrile Neutropenia
12 (.24%)
Hydronephrosis
12 (.24%)
Neuropathy Peripheral
12 (.24%)
Osteoporosis
12 (.24%)
Rash
12 (.24%)
White Blood Cell Count Decreased
12 (.24%)
Asthenia
11 (.22%)
Constipation
11 (.22%)
Dysphagia
11 (.22%)
Feeling Abnormal
11 (.22%)
Fungal Infection
11 (.22%)
Glomerular Filtration Rate Decrease...
11 (.22%)
Hallucination
11 (.22%)
Herpes Simplex
11 (.22%)
Muscular Weakness
11 (.22%)
Pleural Effusion
11 (.22%)

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

What are the most common Steroids Nos adverse events reported to the FDA?

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

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

Renal Transplant
153
Premedication
131
Product Used For Unknown Indication
120
Drug Use For Unknown Indication
102
Rheumatoid Arthritis
44
Liver Transplant
39
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Multiple Sclerosis
36
Bone Marrow Transplant
34
Immunosuppression
32
Nephrotic Syndrome
31
Ill-defined Disorder
26
Multiple Sclerosis Relapse
26
Asthma
26
Crohns Disease
24
Heart Transplant
23
Interstitial Lung Disease
23
Colitis Ulcerative
22
Prophylaxis
18
Stem Cell Transplant
15
Breast Cancer
13
Graft Versus Host Disease
13
Psoriasis
12
Acanthoma
8
Steroid Therapy
7
Pain
7
Dermatomyositis
7
Systemic Lupus Erythematosus
6
Pemphigoid
6
Foetal Exposure During Pregnancy
6
Aplastic Anaemia
6
Chronic Graft Versus Host Disease
5
Cord Blood Transplant Therapy
5
Acute Graft Versus Host Disease
5
Sinusitis
5
Infection
5
Immunosuppressant Drug Therapy
5
Liver And Small Intestine Transplan...
5
Pustular Psoriasis
4
Psoriatic Arthropathy
4
Kidney Transplant Rejection
4
Myasthenia Gravis
4
Prophylaxis Against Transplant Reje...
4
Bone Marrow Transplant Rejection
4
Pruritus
4
Pneumonia
4
Antiinflammatory Therapy
4
Scotoma
4
Pyoderma Gangrenosum
4
Gout
4
Histiocytosis Haematophagic
4
Arthritis
3

Steroids Nos Case Reports

What Steroids Nos 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 Steroids Nos. 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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