NORETHINDRONE ACETATE

N/A

4,107 FDA adverse event reports analyzed

Last updated: 2026-04-15

About NORETHINDRONE ACETATE

NORETHINDRONE ACETATE is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for NORETHINDRONE ACETATE include HOT FLUSH, NAUSEA, HEADACHE, PELVIC PAIN, VAGINAL HAEMORRHAGE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for NORETHINDRONE ACETATE.

Top Adverse Reactions

HOT FLUSH210 reports
NAUSEA152 reports
HEADACHE145 reports
PELVIC PAIN127 reports
VAGINAL HAEMORRHAGE116 reports
ABDOMINAL PAIN110 reports
FATIGUE105 reports
PAIN101 reports
DRUG INEFFECTIVE98 reports
MENORRHAGIA98 reports
ENDOMETRIOSIS95 reports
ARTHRALGIA86 reports
MOOD SWINGS82 reports
INSOMNIA79 reports
MIGRAINE79 reports
DIZZINESS77 reports
BACK PAIN75 reports
OFF LABEL USE73 reports
DEPRESSION72 reports
BREAST CANCER67 reports
DIARRHOEA67 reports
METRORRHAGIA67 reports
ANXIETY62 reports
WEIGHT INCREASED61 reports
MUSCLE SPASMS59 reports
VOMITING56 reports
NIGHT SWEATS49 reports
DYSPNOEA47 reports
ABDOMINAL DISTENSION46 reports
MENSTRUAL DISORDER45 reports
DYSMENORRHOEA42 reports
INJECTION SITE PAIN42 reports
MEMORY IMPAIRMENT41 reports
ALOPECIA38 reports
PAIN IN EXTREMITY37 reports
MENSTRUATION IRREGULAR35 reports
PRODUCT DOSE OMISSION ISSUE35 reports
PYREXIA33 reports
RASH33 reports
ABDOMINAL PAIN UPPER32 reports
FEELING ABNORMAL30 reports
HYPOAESTHESIA29 reports
ABDOMINAL DISCOMFORT28 reports
DECREASED APPETITE28 reports
WEIGHT DECREASED27 reports
HYPERHIDROSIS26 reports
MALAISE26 reports
MOOD ALTERED26 reports
COVID 1925 reports
MYALGIA25 reports
PALPITATIONS25 reports
CRYING24 reports
PRURITUS24 reports
ACNE23 reports
CONDITION AGGRAVATED23 reports
SUICIDAL IDEATION23 reports
BLOOD PRESSURE INCREASED22 reports
HAEMORRHAGE21 reports
HYPERTENSION21 reports
OVARIAN CYST21 reports
PRODUCT USE IN UNAPPROVED INDICATION21 reports
SINUSITIS21 reports
VULVOVAGINAL DRYNESS20 reports
ASTHENIA19 reports
BONE PAIN19 reports
COUGH19 reports
PARAESTHESIA19 reports
UTERINE LEIOMYOMA19 reports
CHEST PAIN18 reports
CONSTIPATION18 reports
SOMNOLENCE18 reports
DRUG DOSE OMISSION17 reports
NASOPHARYNGITIS17 reports
TREMOR17 reports
VISION BLURRED17 reports
ABDOMINAL PAIN LOWER16 reports
ASTHMA16 reports
DYSPAREUNIA16 reports
FALL16 reports
INFLUENZA LIKE ILLNESS16 reports
IRRITABILITY16 reports
URINARY TRACT INFECTION16 reports
ADNEXA UTERI PAIN15 reports
BREAST CANCER METASTATIC15 reports
HYPOTENSION15 reports
CHILLS14 reports
INFLUENZA14 reports
PANIC ATTACK14 reports
PNEUMONIA14 reports
TACHYCARDIA14 reports
VAGINAL DISCHARGE14 reports
AMENORRHOEA13 reports
FEELING HOT13 reports
HYSTERECTOMY13 reports
PRODUCT USE ISSUE13 reports
RHEUMATOID ARTHRITIS13 reports
SEIZURE13 reports
URTICARIA13 reports
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS13 reports
ANGER12 reports

Report Outcomes

Out of 1,600 classified reports for NORETHINDRONE ACETATE:

Serious 40.3%Non-Serious 59.7%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Frequently Asked Questions

How many FDA adverse event reports are associated with NORETHINDRONE ACETATE?

This profile reflects 4,107 FDA FAERS reports that mention NORETHINDRONE ACETATE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for NORETHINDRONE ACETATE?

Frequently reported terms in FAERS include HOT FLUSH, NAUSEA, HEADACHE, PELVIC PAIN, VAGINAL HAEMORRHAGE, ABDOMINAL PAIN. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.