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INTRAUTERINE COPPER CONTRACEPTIVE

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Intrauterine Copper Contraceptive Adverse Events Reported to the FDA Over Time

How are Intrauterine Copper Contraceptive adverse event reports trending over time?

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

Most Common Intrauterine Copper Contraceptive Adverse Events Reported to the FDA

What are the most common Intrauterine Copper Contraceptive adverse events reported to the FDA?

Iucd Complication
59 (10.85%)
Iud Migration
35 (6.43%)
Abdominal Pain
32 (5.88%)
Unintended Pregnancy
28 (5.15%)
Vaginal Haemorrhage
28 (5.15%)
Ectopic Pregnancy
17 (3.13%)
Metrorrhagia
14 (2.57%)
Intra-uterine Contraceptive Device ...
13 (2.39%)
Abortion Spontaneous
12 (2.21%)
Medical Device Complication
12 (2.21%)
Pregnancy With Contraceptive Device
12 (2.21%)
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Menorrhagia
8 (1.47%)
Nausea
7 (1.29%)
Pain
7 (1.29%)
Pelvic Inflammatory Disease
7 (1.29%)
Pelvic Pain
7 (1.29%)
Chorioamnionitis
6 (1.1%)
Dehydration
5 (.92%)
Ovarian Cyst
5 (.92%)
Dizziness
4 (.74%)
Menstruation Irregular
4 (.74%)
Pyrexia
4 (.74%)
Syncope
4 (.74%)
Vaginal Infection
4 (.74%)
Weight Increased
4 (.74%)
Abdominal Discomfort
3 (.55%)
Abdominal Distension
3 (.55%)
Abdominal Pain Lower
3 (.55%)
Abscess
3 (.55%)
Anaemia
3 (.55%)
Asthenia
3 (.55%)
Caesarean Section
3 (.55%)
Constipation
3 (.55%)
Device Dislocation
3 (.55%)
Drug Exposure During Pregnancy
3 (.55%)
Dysmenorrhoea
3 (.55%)
Malaise
3 (.55%)
Meningitis
3 (.55%)
Menstruation Delayed
3 (.55%)
Pruritus
3 (.55%)
Pyelonephritis
3 (.55%)
Sinusitis
3 (.55%)
Stillbirth
3 (.55%)
Tubo-ovarian Abscess
3 (.55%)
Uterine Contractions During Pregnan...
3 (.55%)
Uterine Haemorrhage
3 (.55%)
Abdominal Adhesions
2 (.37%)
Abortion Infected
2 (.37%)
Back Pain
2 (.37%)
Beta Haemolytic Streptococcal Infec...
2 (.37%)
Breech Presentation
2 (.37%)
Chills
2 (.37%)
Complication Of Device Removal
2 (.37%)
Disease Recurrence
2 (.37%)
Disseminated Intravascular Coagulat...
2 (.37%)
Endometritis
2 (.37%)
Erythema
2 (.37%)
Fallopian Tube Disorder
2 (.37%)
Headache
2 (.37%)
Hypomenorrhoea
2 (.37%)
Infection
2 (.37%)
Intra-uterine Death
2 (.37%)
Medical Device Pain
2 (.37%)
Photosensitivity Allergic Reaction
2 (.37%)
Pregnancy
2 (.37%)
Sciatica
2 (.37%)
Urinary Tract Infection
2 (.37%)
Uterine Leiomyoma
2 (.37%)
Uterine Polyp
2 (.37%)
Abdominal Abscess
1 (.18%)
Abortion
1 (.18%)
Abortion Induced
1 (.18%)
Adhesion
1 (.18%)
Alopecia
1 (.18%)
Amenorrhoea
1 (.18%)
Amniotic Fluid Volume Increased
1 (.18%)
Anorectal Disorder
1 (.18%)
Ascites
1 (.18%)
Back Injury
1 (.18%)
Breast Cancer Female
1 (.18%)
Bronchitis
1 (.18%)
Calculus Bladder
1 (.18%)
Candidiasis
1 (.18%)
Cervical Dysplasia
1 (.18%)
Chest Pain
1 (.18%)
Cholelithiasis
1 (.18%)
Cold Sweat
1 (.18%)
Convulsion
1 (.18%)
Csf Glucose Decreased
1 (.18%)
Csf Pressure Increased
1 (.18%)
Csf Protein Increased
1 (.18%)
Csf White Blood Cell Count Increase...
1 (.18%)
Depressed Level Of Consciousness
1 (.18%)
Device Breakage
1 (.18%)
Device Failure
1 (.18%)
Device Related Infection
1 (.18%)
Discomfort
1 (.18%)
Disorientation
1 (.18%)
Drug Ineffective
1 (.18%)
Dysarthria
1 (.18%)
Dysgeusia
1 (.18%)

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This graph shows the top adverse events submitted to the FDA for Intrauterine Copper Contraceptive, 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 Intrauterine Copper Contraceptive 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 Intrauterine Copper Contraceptive

What are the most common Intrauterine Copper Contraceptive adverse events reported to the FDA?

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

Why are people taking Intrauterine Copper Contraceptive, according to those reporting adverse events to the FDA?

Contraception
211
Drug Use For Unknown Indication
2

Intrauterine Copper Contraceptive Case Reports

What Intrauterine Copper Contraceptive 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 Intrauterine Copper Contraceptive. 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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