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Micronor Adverse Events Reported to the FDA Over Time

How are Micronor adverse event reports trending over time?

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

Most Common Micronor Adverse Events Reported to the FDA

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

Drug Exposure During Pregnancy
46 (6.43%)
Pregnancy On Oral Contraceptive
45 (6.29%)
Vaginal Haemorrhage
41 (5.73%)
Inappropriate Schedule Of Drug Admi...
20 (2.8%)
Headache
19 (2.66%)
Abdominal Pain
17 (2.38%)
Suppressed Lactation
13 (1.82%)
Drug Exposure Via Breast Milk
12 (1.68%)
Weight Decreased
12 (1.68%)
Depression
11 (1.54%)
Abortion Spontaneous
10 (1.4%)
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Drug Dose Omission
10 (1.4%)
Abdominal Distension
9 (1.26%)
Dizziness
8 (1.12%)
Drug Interaction
8 (1.12%)
Migraine
8 (1.12%)
Anxiety
7 (.98%)
Metrorrhagia
7 (.98%)
Nervousness
7 (.98%)
Uterine Spasm
7 (.98%)
Asthenia
6 (.84%)
Lupus-like Syndrome
6 (.84%)
Medication Error
6 (.84%)
Product Quality Issue
6 (.84%)
Smear Vaginal Abnormal
6 (.84%)
Syncope
6 (.84%)
Tremor
6 (.84%)
Vision Blurred
6 (.84%)
Abdominal Discomfort
5 (.7%)
Nausea
5 (.7%)
Pulmonary Embolism
5 (.7%)
Accidental Drug Intake By Child
4 (.56%)
Arthritis
4 (.56%)
Breast Cancer
4 (.56%)
Breast Pain
4 (.56%)
Ectopic Pregnancy
4 (.56%)
Hyperlipidaemia
4 (.56%)
Mood Altered
4 (.56%)
Myalgia
4 (.56%)
Premenstrual Syndrome
4 (.56%)
Psoriatic Arthropathy
4 (.56%)
Rash
4 (.56%)
Somnolence
4 (.56%)
Weight Increased
4 (.56%)
Abdominal Pain Upper
3 (.42%)
Amenorrhoea
3 (.42%)
Anaemia
3 (.42%)
Back Pain
3 (.42%)
Cerebrovascular Accident
3 (.42%)
Cyst
3 (.42%)
Dysmenorrhoea
3 (.42%)
Fatigue
3 (.42%)
Grand Mal Convulsion
3 (.42%)
Haemorrhage
3 (.42%)
Hospitalisation
3 (.42%)
Hypotension
3 (.42%)
International Normalised Ratio Incr...
3 (.42%)
Irritability
3 (.42%)
Lactose Intolerance
3 (.42%)
Musculoskeletal Stiffness
3 (.42%)
Off Label Use
3 (.42%)
Pelvic Pain
3 (.42%)
Photophobia
3 (.42%)
Premature Baby
3 (.42%)
Superior Sagittal Sinus Thrombosis
3 (.42%)
Transverse Sinus Thrombosis
3 (.42%)
Urinary Tract Infection
3 (.42%)
Abortion Spontaneous Incomplete
2 (.28%)
Acne
2 (.28%)
Arthralgia
2 (.28%)
Bladder Discomfort
2 (.28%)
Cardiac Arrest
2 (.28%)
Cholelithiasis
2 (.28%)
Completed Suicide
2 (.28%)
Contusion
2 (.28%)
Convulsion
2 (.28%)
Cystitis
2 (.28%)
Cystitis Noninfective
2 (.28%)
Depressed Mood
2 (.28%)
Depression Suicidal
2 (.28%)
Diarrhoea
2 (.28%)
Emotional Disorder
2 (.28%)
Episcleritis
2 (.28%)
Failure To Thrive
2 (.28%)
Gallbladder Operation
2 (.28%)
Gastrooesophageal Reflux Disease
2 (.28%)
Hypertension
2 (.28%)
Hypertensive Crisis
2 (.28%)
Hypothyroidism
2 (.28%)
Intra-uterine Death
2 (.28%)
Jaundice Cholestatic
2 (.28%)
Joint Swelling
2 (.28%)
Limb Reduction Defect
2 (.28%)
Loss Of Consciousness
2 (.28%)
Macular Degeneration
2 (.28%)
Menopausal Symptoms
2 (.28%)
Menstrual Disorder
2 (.28%)
Muscular Weakness
2 (.28%)
Panic Attack
2 (.28%)
Pyrexia
2 (.28%)
Rash Pruritic
2 (.28%)

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

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

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

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

Contraception
181
Drug Use For Unknown Indication
49
Hormone Replacement Therapy
19
Drug Exposure Via Breast Milk
12
Oral Contraception
8
Product Used For Unknown Indication
7
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Drug Exposure During Pregnancy
5
Dysmenorrhoea
4
Accidental Exposure
3
Menorrhagia
3
Vaginal Haemorrhage
1
Endometriosis
1
Menometrorrhagia
1
Accidental Drug Intake By Child
1
Migraine
1
Investigation
1
Menopausal Symptoms
1
Endometrial Hyperplasia
1

Drug Labels

LabelLabelerEffective
Ortho MicronorOrtho-McNeil-Janssen Pharmaceuticals, Inc.01-JUL-08
MicronorPhysicians Total Care, Inc.01-APR-11
Ortho MicronorJanssen Pharmaceuticals, Inc.28-FEB-13

Micronor Case Reports

What Micronor 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 Micronor. 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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