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DEXAMETHASONE SODIUM PHOSPHATE

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Dexamethasone Sodium Phosphate Adverse Events Reported to the FDA Over Time

How are Dexamethasone Sodium Phosphate adverse event reports trending over time?

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

Most Common Dexamethasone Sodium Phosphate Adverse Events Reported to the FDA

What are the most common Dexamethasone Sodium Phosphate adverse events reported to the FDA?

Pneumonia
1145 (1.49%)
Pyrexia
1024 (1.33%)
Neutropenia
984 (1.28%)
Diarrhoea
909 (1.18%)
Thrombocytopenia
865 (1.12%)
Sepsis
760 (.99%)
Dyspnoea
695 (.9%)
Fatigue
695 (.9%)
Anaemia
684 (.89%)
Febrile Neutropenia
678 (.88%)
Nausea
606 (.79%)
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Platelet Count Decreased
605 (.79%)
Death
603 (.78%)
Haemoglobin Decreased
592 (.77%)
Vomiting
591 (.77%)
Hypotension
579 (.75%)
Dehydration
548 (.71%)
Asthenia
541 (.7%)
Disease Progression
519 (.67%)
Renal Failure Acute
498 (.65%)
Multiple Myeloma
494 (.64%)
Infection
487 (.63%)
Deep Vein Thrombosis
474 (.62%)
Pancytopenia
468 (.61%)
Renal Failure
454 (.59%)
Pulmonary Embolism
445 (.58%)
Constipation
440 (.57%)
Neuropathy Peripheral
436 (.57%)
General Physical Health Deteriorati...
425 (.55%)
Confusional State
393 (.51%)
Atrial Fibrillation
389 (.5%)
Hyperglycaemia
388 (.5%)
Abdominal Pain
386 (.5%)
White Blood Cell Count Decreased
373 (.48%)
Pleural Effusion
360 (.47%)
Septic Shock
360 (.47%)
Respiratory Failure
357 (.46%)
Pain
304 (.39%)
Hyponatraemia
300 (.39%)
Rash
298 (.39%)
Dizziness
297 (.39%)
Chest Pain
290 (.38%)
Multi-organ Failure
282 (.37%)
Headache
278 (.36%)
Oedema Peripheral
275 (.36%)
Blood Creatinine Increased
269 (.35%)
Back Pain
268 (.35%)
Leukopenia
257 (.33%)
Hypokalaemia
255 (.33%)
Drug Ineffective
251 (.33%)
Neutrophil Count Decreased
242 (.31%)
Cough
230 (.3%)
Convulsion
228 (.3%)
Haemorrhage
228 (.3%)
Hypoxia
228 (.3%)
Alanine Aminotransferase Increased
226 (.29%)
Malaise
223 (.29%)
Condition Aggravated
222 (.29%)
Tachycardia
221 (.29%)
Hypertension
216 (.28%)
Mucosal Inflammation
214 (.28%)
Decreased Appetite
213 (.28%)
Fall
204 (.26%)
Muscular Weakness
204 (.26%)
Drug Interaction
203 (.26%)
Somnolence
202 (.26%)
Osteonecrosis
201 (.26%)
Cardiac Failure
199 (.26%)
Gastrointestinal Haemorrhage
196 (.25%)
Syncope
194 (.25%)
Aspartate Aminotransferase Increase...
193 (.25%)
Tumour Lysis Syndrome
192 (.25%)
Malignant Neoplasm Progression
191 (.25%)
Pain In Extremity
188 (.24%)
Lung Disorder
185 (.24%)
Arthralgia
183 (.24%)
Chills
181 (.23%)
Herpes Zoster
181 (.23%)
Blood Glucose Increased
180 (.23%)
Staphylococcal Infection
179 (.23%)
Myelodysplastic Syndrome
177 (.23%)
Cardiac Arrest
175 (.23%)
Hypocalcaemia
175 (.23%)
Thrombosis
174 (.23%)
Urinary Tract Infection
174 (.23%)
Drug Toxicity
171 (.22%)
Insomnia
171 (.22%)
Weight Decreased
171 (.22%)
Haematocrit Decreased
167 (.22%)
Cellulitis
164 (.21%)
C-reactive Protein Increased
163 (.21%)
Hypoaesthesia
155 (.2%)
Renal Impairment
150 (.19%)
Pulmonary Oedema
149 (.19%)
Mental Status Changes
147 (.19%)
Acute Respiratory Distress Syndrome
146 (.19%)
Blood Lactate Dehydrogenase Increas...
146 (.19%)
Atelectasis
145 (.19%)
Colitis
144 (.19%)
Agitation
143 (.19%)
International Normalised Ratio Incr...
142 (.18%)

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This graph shows the top adverse events submitted to the FDA for Dexamethasone Sodium Phosphate, 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 Dexamethasone Sodium Phosphate 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 Dexamethasone Sodium Phosphate

What are the most common Dexamethasone Sodium Phosphate adverse events reported to the FDA?

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

Why are people taking Dexamethasone Sodium Phosphate, according to those reporting adverse events to the FDA?

Multiple Myeloma
9671
Drug Use For Unknown Indication
1850
Premedication
1768
Prophylaxis
1414
Product Used For Unknown Indication
1121
Acute Lymphocytic Leukaemia
784
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Prophylaxis Of Nausea And Vomiting
542
Nausea
385
Mantle Cell Lymphoma
333
Antiemetic Supportive Care
296
Non-hodgkins Lymphoma
255
Amyloidosis
226
Chemotherapy
203
Chronic Lymphocytic Leukaemia
178
Lymphoma
168
Vomiting
144
B-cell Lymphoma
140
Prostate Cancer
136
Brain Oedema
124
Pain
117
Metastases To Central Nervous Syste...
117
Diffuse Large B-cell Lymphoma
115
Supplementation Therapy
106
Plasmacytoma
97
Myeloma Recurrence
81
Burkitts Lymphoma
77
Breast Cancer
66
Diffuse Large B-cell Lymphoma Recur...
65
Glioblastoma Multiforme
59
Leukaemia Plasmacytic
54
B Precursor Type Acute Leukaemia
54
Histiocytosis Haematophagic
53
Inflammation
49
Antiinflammatory Therapy
48
Rheumatoid Arthritis
46
Waldenstroms Macroglobulinaemia
45
Oedema
44
Prostate Cancer Stage Iv
44
Acute Myeloid Leukaemia
43
Primary Amyloidosis
43
T-cell Lymphoma Stage Iv
42
Fatigue
42
Prophylactic Chemotherapy
41
Ill-defined Disorder
40
Dyspnoea
39
Asthma
38
Postoperative Care
38
T-cell Lymphoma
37
Peripheral T-cell Lymphoma Unspecif...
37
Glioblastoma
37
T-cell Type Acute Leukaemia
36

Drug Labels

LabelLabelerEffective
Dexamethasone Sodium PhosphatePhysicians Total Care, Inc.09-OCT-09
Dexamethasone Sodium Phosphate Stat Rx USA27-OCT-09
Dexamethasone Sodium PhosphateBausch & Lomb Incorporated18-AUG-10
Dexamethasone Sodium PhosphateGeneral Injectables & Vaccines26-AUG-10
Dexamethasone Sodium PhosphatesAmerican Regent, Inc.08-SEP-10
Dexamethasone Sodium PhosphateButler Animal Health Supply04-NOV-10
Dexamethasone Sodium PhosphatePhoenix Pharmaceutical, Inc.04-NOV-10
Dexamethasone Sodium PhosphateMajor Pharmaceuticals15-DEC-10
Dexamethasone Sodium PhosphateRebel Distributors Corp16-DEC-10
Dexamethasone Sodium PhosphatePhysicians Total Care, Inc.13-JAN-11
Dexamethasone Sodium PhosphateGeneral Injectables & Vaccines13-JAN-11
Dexamethasone Sodium PhosphatePhysicians Total Care, Inc.13-JAN-11
Dexamethasone Sodium PhosphateFalcon Pharmaceuticals12-JUL-11
Dexamethasone Sodium PhosphateGeneral Injectables & Vaccines, Inc.18-JUL-11
Dexamethasone Sodium PhosphateAPP Pharmaceuticals, LLC22-AUG-11
Dexamethasone Sodium PhosphatePfizer Laboratories Div Pfizer Inc06-SEP-11
Dexamethasone Sodium PhosphatesCardinal Health08-SEP-11
Dexamethasone Sodium PhosphateWest-ward Pharmaceutical Corp.16-SEP-11
Dexamethasone Sodium PhosphateDispensing Solutions, Inc.03-OCT-11
Dexamethasone Sodium PhosphateRebel Distributors Corp27-DEC-11
Dexamethasone Sodium PhosphateAPP Pharmaceuticals, LLC05-JAN-12
Dexamethasone Sodium PhosphateGeneral Injectables & Vaccines, Inc30-MAR-12
Dexamethasone Sodium PhosphateCardinal Health20-APR-12
Dexamethasone Sodium PhosphateCardinal Health02-AUG-12
Dexamethasone Sodium PhosphateCardinal Health16-AUG-12
Dexamethasone Sodium PhosphateCardinal Health18-APR-13
Dexamethasone Sodium PhosphateCardinal Health26-APR-13
Dexamethasone Sodium PhosphateCardinal Health26-APR-13
Dexamethasone Sodium PhosphateCardinal Health30-APR-13

Dexamethasone Sodium Phosphate Case Reports

What Dexamethasone Sodium Phosphate 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 Dexamethasone Sodium Phosphate. 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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