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LUPRON DEPOT PED

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Lupron Depot Ped Adverse Events Reported to the FDA Over Time

How are Lupron Depot Ped adverse event reports trending over time?

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

Most Common Lupron Depot Ped Adverse Events Reported to the FDA

What are the most common Lupron Depot Ped adverse events reported to the FDA?

Injection Site Pain
27 (4.1%)
Drug Dispensing Error
23 (3.5%)
Headache
21 (3.19%)
Incorrect Dose Administered
19 (2.89%)
Pyrexia
18 (2.74%)
Injection Site Abscess
17 (2.58%)
Weight Increased
15 (2.28%)
Injection Site Erythema
13 (1.98%)
Arthralgia
12 (1.82%)
Drug Ineffective
12 (1.82%)
Drug Dose Omission
11 (1.67%)
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Gait Disturbance
10 (1.52%)
Pain In Extremity
10 (1.52%)
Convulsion
8 (1.22%)
Dizziness
8 (1.22%)
Dyspnoea
8 (1.22%)
Injection Site Abscess Sterile
8 (1.22%)
Injection Site Reaction
8 (1.22%)
Pain
8 (1.22%)
Injection Site Nodule
7 (1.06%)
Injection Site Swelling
7 (1.06%)
Crying
6 (.91%)
Dysacusis
6 (.91%)
Hyperacusis
6 (.91%)
Nausea
6 (.91%)
Rash
6 (.91%)
Wrong Drug Administered
6 (.91%)
Diarrhoea
5 (.76%)
Hot Flush
5 (.76%)
Mood Swings
5 (.76%)
Overdose
5 (.76%)
Urticaria
5 (.76%)
Vomiting
5 (.76%)
Abasia
4 (.61%)
Breast Enlargement
4 (.61%)
Feeling Hot
4 (.61%)
Growth Accelerated
4 (.61%)
Hypersensitivity
4 (.61%)
Hypertension
4 (.61%)
Infection
4 (.61%)
Injection Site Discomfort
4 (.61%)
Mobility Decreased
4 (.61%)
Neuropathy Peripheral
4 (.61%)
Oedema Peripheral
4 (.61%)
Off Label Use
4 (.61%)
Abnormal Behaviour
3 (.46%)
Abscess
3 (.46%)
Balance Disorder
3 (.46%)
Body Height Increased
3 (.46%)
Csf Protein Increased
3 (.46%)
Death
3 (.46%)
Depression
3 (.46%)
Drug Effect Decreased
3 (.46%)
Drug Prescribing Error
3 (.46%)
Fall
3 (.46%)
Inappropriate Schedule Of Drug Admi...
3 (.46%)
Incorrect Drug Dosage Form Administ...
3 (.46%)
Injection Site Induration
3 (.46%)
Metrorrhagia
3 (.46%)
Muscle Spasms
3 (.46%)
Myalgia
3 (.46%)
Papilloedema
3 (.46%)
Personality Change
3 (.46%)
Rash Papular
3 (.46%)
Rash Pruritic
3 (.46%)
Urinary Tract Infection
3 (.46%)
Vaginal Haemorrhage
3 (.46%)
Viral Infection
3 (.46%)
Abdominal Pain
2 (.3%)
Acne
2 (.3%)
Aggression
2 (.3%)
Alopecia
2 (.3%)
Anger
2 (.3%)
Areflexia
2 (.3%)
Blood Testosterone Abnormal
2 (.3%)
Bone Cyst
2 (.3%)
C-reactive Protein Increased
2 (.3%)
Cauda Equina Syndrome
2 (.3%)
Chest Pain
2 (.3%)
Contusion
2 (.3%)
Cough
2 (.3%)
Demyelinating Polyneuropathy
2 (.3%)
Disorientation
2 (.3%)
Disturbance In Attention
2 (.3%)
Emotional Disorder
2 (.3%)
Fatigue
2 (.3%)
Feeling Abnormal
2 (.3%)
Generalised Erythema
2 (.3%)
Guillain-barre Syndrome
2 (.3%)
Hair Disorder
2 (.3%)
Ill-defined Disorder
2 (.3%)
Injection Site Haemorrhage
2 (.3%)
Injection Site Mass
2 (.3%)
Injection Site Pruritus
2 (.3%)
Injection Site Urticaria
2 (.3%)
Joint Swelling
2 (.3%)
Latent Tuberculosis
2 (.3%)
Limb Discomfort
2 (.3%)
Loss Of Consciousness
2 (.3%)
Malaise
2 (.3%)
Medication Error
2 (.3%)

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This graph shows the top adverse events submitted to the FDA for Lupron Depot Ped, 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 Lupron Depot Ped 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 Lupron Depot Ped

What are the most common Lupron Depot Ped adverse events reported to the FDA?

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

Why are people taking Lupron Depot Ped, according to those reporting adverse events to the FDA?

Precocious Puberty
186
Product Used For Unknown Indication
27
Drug Use For Unknown Indication
11
Uterine Leiomyoma
4
Endometriosis
3
Menorrhagia
2
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Transgender Operation
1
Ovarian Cyst
1
Blood Growth Hormone
1
Prostate Cancer
1
Breast Enlargement
1
Body Height Abnormal
1
Hormone Level Abnormal
1
Vaginal Haemorrhage
1
Underweight
1
Menstrual Disorder
1
Drug Therapy Changed
1
Body Height Below Normal
1
Bone Development Abnormal
1
Puberty
1
Hormone Suppression Therapy
1

Drug Labels

LabelLabelerEffective
Lupron Depot PedTakeda Pharmaceutical Company LTD07-JAN-11
Lupron Depot-pedAbbott Laboratories17-AUG-11
Lupron Depot-pedAbbott Laboratories13-OCT-11

Lupron Depot Ped Case Reports

What Lupron Depot Ped 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 Lupron Depot Ped. 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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