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Neupogen Adverse Events Reported to the FDA Over Time

How are Neupogen adverse event reports trending over time?

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

Most Common Neupogen Adverse Events Reported to the FDA

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

Neutropenia
318 (2.24%)
Febrile Neutropenia
296 (2.08%)
Pyrexia
291 (2.05%)
White Blood Cell Count Decreased
223 (1.57%)
Bone Pain
221 (1.55%)
Drug Ineffective
213 (1.5%)
Dyspnoea
199 (1.4%)
Nausea
175 (1.23%)
Pneumonia
172 (1.21%)
Fatigue
147 (1.03%)
Back Pain
144 (1.01%)
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Diarrhoea
143 (1.01%)
Anaemia
134 (.94%)
Pain
134 (.94%)
Death
130 (.91%)
Vomiting
122 (.86%)
Infection
119 (.84%)
Platelet Count Decreased
118 (.83%)
Headache
117 (.82%)
Rash
113 (.79%)
Thrombocytopenia
110 (.77%)
Malaise
109 (.77%)
Arthralgia
102 (.72%)
Asthenia
101 (.71%)
Sepsis
99 (.7%)
White Blood Cell Count Increased
95 (.67%)
Weight Decreased
94 (.66%)
Haemoglobin Decreased
92 (.65%)
Pancytopenia
92 (.65%)
Leukopenia
90 (.63%)
Neutrophil Count Decreased
90 (.63%)
Deep Vein Thrombosis
89 (.63%)
Dehydration
89 (.63%)
Dizziness
83 (.58%)
Chest Pain
74 (.52%)
Myalgia
73 (.51%)
Acute Myeloid Leukaemia
71 (.5%)
Confusional State
70 (.49%)
Abdominal Pain
69 (.48%)
Pleural Effusion
69 (.48%)
Hypotension
66 (.46%)
Hypersensitivity
65 (.46%)
Injection Site Pain
65 (.46%)
Pain In Extremity
65 (.46%)
Pulmonary Embolism
65 (.46%)
Chills
60 (.42%)
Cough
60 (.42%)
Septic Shock
60 (.42%)
Myelodysplastic Syndrome
57 (.4%)
Therapeutic Response Decreased
57 (.4%)
Acute Respiratory Distress Syndrome
56 (.39%)
Lung Infiltration
54 (.38%)
Pruritus
54 (.38%)
Alopecia
53 (.37%)
Insomnia
50 (.35%)
Leukocytosis
50 (.35%)
Agranulocytosis
49 (.34%)
General Physical Health Deteriorati...
49 (.34%)
Syncope
47 (.33%)
Delirium
45 (.32%)
Interstitial Lung Disease
45 (.32%)
Hyperhidrosis
44 (.31%)
Stomatitis
44 (.31%)
Petechiae
43 (.3%)
Influenza Like Illness
42 (.3%)
Renal Failure Acute
42 (.3%)
Body Temperature Increased
41 (.29%)
Tachycardia
41 (.29%)
Chest Discomfort
40 (.28%)
Neutropenic Sepsis
40 (.28%)
Oedema Peripheral
39 (.27%)
Respiratory Failure
39 (.27%)
Loss Of Consciousness
38 (.27%)
Myocardial Infarction
38 (.27%)
Renal Failure
38 (.27%)
Dermatitis Allergic
37 (.26%)
Muscle Spasms
37 (.26%)
Splenomegaly
37 (.26%)
Urinary Tract Infection
37 (.26%)
Atrial Fibrillation
36 (.25%)
Hypokalaemia
35 (.25%)
Musculoskeletal Pain
35 (.25%)
Cytokine Storm
34 (.24%)
Mucosal Inflammation
34 (.24%)
Multi-organ Failure
34 (.24%)
Neutrophil Count Increased
33 (.23%)
Pulmonary Fibrosis
33 (.23%)
Urticaria
33 (.23%)
Cellulitis
32 (.22%)
Feeling Abnormal
32 (.22%)
Lung Disorder
32 (.22%)
Depression
31 (.22%)
Erythema
31 (.22%)
Impetigo
31 (.22%)
Abdominal Pain Upper
29 (.2%)
Cardiac Failure
29 (.2%)
Haematuria
28 (.2%)
Proteinuria
28 (.2%)
Red Blood Cell Count Decreased
28 (.2%)
Acute Febrile Neutrophilic Dermatos...
27 (.19%)
Oral Candidiasis
27 (.19%)

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

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

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

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

Neutropenia
951
Chemotherapy
835
Drug Use For Unknown Indication
630
Product Used For Unknown Indication
464
Diffuse Large B-cell Lymphoma
426
Prophylaxis
199
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Peripheral Blood Stem Cell Apheresi...
152
Acute Myeloid Leukaemia
135
Haematopoietic Stem Cell Mobilisati...
120
Blood Stem Cell Harvest
113
Myelodysplastic Syndrome
85
Agranulocytosis
74
White Blood Cell Count Decreased
63
Aplastic Anaemia
53
B-cell Lymphoma
51
Leukopenia
50
Multiple Myeloma
45
Hodgkins Disease
39
Neutrophil Count Decreased
38
Breast Cancer
38
Pre-existing Disease
35
Pancytopenia
31
Anaemia
30
Febrile Neutropenia
28
Non-hodgkins Lymphoma
28
Granulocyte Count Decreased
26
Acute Lymphocytic Leukaemia
24
Bone Marrow Transplant
22
Malignant Lymphoid Neoplasm
20
Infection Prophylaxis
19
Hepatitis C
18
Granulocytopenia
18
Colony Stimulating Factor Therapy
17
Mantle Cell Lymphoma
16
Peripheral T-cell Lymphoma Unspecif...
14
Palliative Care
14
Malignant Melanoma
13
Colony Stimulating Factor Prophylax...
13
Stem Cell Transplant
13
Lymphoma
11
Burkitts Lymphoma
11
Chronic Myeloid Leukaemia
9
T-cell Lymphoma
9
Infantile Genetic Agranulocytosis
9
Bone Marrow Failure
9
Idiopathic Neutropenia
9
Cyclic Neutropenia
9
Acute Myeloid Leukaemia Recurrent
8
Bone Marrow Conditioning Regimen
8
Neoplasm Malignant
7
Blood Count Abnormal
7

Drug Labels

LabelLabelerEffective
NeupogenPhysicians Total Care, Inc.02-DEC-09
NeupogenAmgen Inc05-MAR-13

Neupogen Case Reports

What Neupogen 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 Neupogen. 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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