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PANITUMUMAB

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Panitumumab Adverse Events Reported to the FDA Over Time

How are Panitumumab adverse event reports trending over time?

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

Most Common Panitumumab Adverse Events Reported to the FDA

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

Diarrhoea
605 (4.12%)
Dermatitis Acneiform
595 (4.05%)
Dehydration
428 (2.91%)
Stomatitis
420 (2.86%)
Colorectal Cancer
372 (2.53%)
Interstitial Lung Disease
310 (2.11%)
Febrile Neutropenia
277 (1.88%)
Hypomagnesaemia
276 (1.88%)
Paronychia
249 (1.69%)
Decreased Appetite
232 (1.58%)
Pyrexia
229 (1.56%)
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Vomiting
215 (1.46%)
Dry Skin
203 (1.38%)
Neutropenia
199 (1.35%)
Nausea
196 (1.33%)
Rash
193 (1.31%)
Pneumonia
169 (1.15%)
Anaemia
164 (1.12%)
Hypocalcaemia
159 (1.08%)
Hypokalaemia
152 (1.03%)
Fatigue
139 (.95%)
Pulmonary Embolism
139 (.95%)
White Blood Cell Count Decreased
127 (.86%)
Neutrophil Count Decreased
120 (.82%)
Mucosal Inflammation
116 (.79%)
Dyspnoea
115 (.78%)
Malaise
114 (.78%)
Asthenia
113 (.77%)
Death
109 (.74%)
Sepsis
108 (.73%)
Hypotension
101 (.69%)
Deep Vein Thrombosis
96 (.65%)
Infection
89 (.61%)
Thrombocytopenia
88 (.6%)
Pruritus
86 (.59%)
General Physical Health Deteriorati...
81 (.55%)
Dermatitis
78 (.53%)
Renal Failure Acute
78 (.53%)
Acne
77 (.52%)
Pancytopenia
73 (.5%)
Hyponatraemia
69 (.47%)
Platelet Count Decreased
69 (.47%)
Neutropenic Sepsis
68 (.46%)
Haemoglobin Decreased
66 (.45%)
Abdominal Pain
62 (.42%)
Anorexia
61 (.41%)
Intestinal Obstruction
60 (.41%)
Urinary Tract Infection
60 (.41%)
Atrial Fibrillation
59 (.4%)
Renal Failure
58 (.39%)
Dysphagia
57 (.39%)
Infusion Related Reaction
53 (.36%)
Weight Decreased
53 (.36%)
Dizziness
52 (.35%)
Ileus
51 (.35%)
Malignant Neoplasm Progression
49 (.33%)
Hepatic Function Abnormal
48 (.33%)
Blood Creatinine Increased
47 (.32%)
Disease Progression
47 (.32%)
Pleural Effusion
46 (.31%)
Thrombosis
46 (.31%)
Neuropathy Peripheral
45 (.31%)
Leukopenia
44 (.3%)
Blood Magnesium Decreased
43 (.29%)
Gastrointestinal Haemorrhage
43 (.29%)
Cerebral Infarction
42 (.29%)
Respiratory Failure
42 (.29%)
Chills
40 (.27%)
Oedema Peripheral
40 (.27%)
Back Pain
39 (.27%)
Hyperkalaemia
39 (.27%)
Hypoalbuminaemia
39 (.27%)
Electrolyte Imbalance
38 (.26%)
Syncope
38 (.26%)
Cellulitis
37 (.25%)
Convulsion
37 (.25%)
Blood Calcium Decreased
36 (.24%)
Folliculitis
36 (.24%)
Hypersensitivity
36 (.24%)
Confusional State
35 (.24%)
Multi-organ Failure
34 (.23%)
Blood Sodium Decreased
33 (.22%)
Hypoxia
33 (.22%)
Skin Fissures
33 (.22%)
Small Intestinal Obstruction
32 (.22%)
Venous Thrombosis
32 (.22%)
Chest Pain
31 (.21%)
Glossitis
31 (.21%)
Haematocrit Decreased
31 (.21%)
Erythema
30 (.2%)
Disseminated Intravascular Coagulat...
29 (.2%)
Pain
29 (.2%)
Ascites
28 (.19%)
Colitis
28 (.19%)
Intestinal Perforation
28 (.19%)
Septic Shock
28 (.19%)
Blood Potassium Decreased
27 (.18%)
Dysgeusia
27 (.18%)
Lethargy
27 (.18%)
Pneumonitis
27 (.18%)
Alanine Aminotransferase Increased
26 (.18%)

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

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

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

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

Colorectal Cancer
2401
Squamous Cell Carcinoma
485
Colorectal Cancer Metastatic
226
Gastrooesophageal Cancer
93
Oesophageal Carcinoma
71
Pancreatic Carcinoma
58
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Oesophageal Adenocarcinoma
38
Metastatic Neoplasm
36
Neoplasm Malignant
35
Head And Neck Cancer
33
Non-small Cell Lung Cancer
27
Colon Cancer
26
Gastric Cancer
25
Colon Cancer Metastatic
24
Transitional Cell Carcinoma
22
Adenocarcinoma Pancreas
20
Breast Cancer
19
Anal Cancer
18
Breast Cancer Metastatic
11
Large Intestine Carcinoma
11
Rectal Cancer Metastatic
9
Drug Use For Unknown Indication
9
Pancreatic Carcinoma Metastatic
8
Bile Duct Cancer
8
Oropharyngeal Cancer Stage Unspecif...
7
Rectal Cancer
7
Neoplasm
6
Small Intestine Carcinoma Metastati...
5
Product Used For Unknown Indication
4
Prophylaxis
4
Ovarian Cancer
3
Renal Cell Carcinoma Stage Unspecif...
3
Tongue Neoplasm Malignant Stage Uns...
2
Tonsil Cancer
2
Head And Neck Cancer Metastatic
2
Colon Cancer Stage Iv
1
Gallbladder Cancer
1
Lung Squamous Cell Carcinoma Stage ...
1
Rectal Cancer Recurrent
1
Pneumonia Aspiration
1
Hepatic Cancer Metastatic
1
Lung Neoplasm Malignant
1
Neuroendocrine Tumour
1
Pre-existing Disease
1
Signet-ring Cell Carcinoma
1

Drug Labels

LabelLabelerEffective
VectibixAmgen Inc28-MAR-13

Panitumumab Case Reports

What Panitumumab 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 Panitumumab. 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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