ANASTROZOLE TABLETS

N/A

Manufactured by Avet Pharmaceuticals Inc

50,885 FDA adverse event reports analyzed

Last updated: 2026-04-14

About ANASTROZOLE TABLETS

ANASTROZOLE TABLETS is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Avet Pharmaceuticals Inc. The most commonly reported adverse reactions for ANASTROZOLE TABLETS include FATIGUE, NAUSEA, DIARRHOEA, ARTHRALGIA, ALOPECIA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ANASTROZOLE TABLETS.

Top Adverse Reactions

FATIGUE2,185 reports
NAUSEA1,761 reports
DIARRHOEA1,676 reports
ARTHRALGIA1,504 reports
ALOPECIA1,386 reports
HEADACHE1,119 reports
DYSPNOEA1,034 reports
ASTHENIA991 reports
MALIGNANT NEOPLASM PROGRESSION980 reports
DIZZINESS965 reports
PAIN961 reports
VOMITING937 reports
DRUG INEFFECTIVE841 reports
OFF LABEL USE834 reports
MALAISE826 reports
DECREASED APPETITE822 reports
COUGH790 reports
PRURITUS753 reports
METASTASES TO BONE742 reports
WHITE BLOOD CELL COUNT DECREASED742 reports
NEUTROPENIA736 reports
INSOMNIA696 reports
PAIN IN EXTREMITY665 reports
FALL652 reports
BREAST CANCER637 reports
RASH585 reports
MYALGIA579 reports
PYREXIA574 reports
CONSTIPATION542 reports
ABDOMINAL PAIN528 reports
WEIGHT DECREASED521 reports
HOT FLUSH505 reports
DEATH501 reports
BONE PAIN483 reports
ANXIETY479 reports
BACK PAIN475 reports
ABDOMINAL PAIN UPPER473 reports
DISEASE PROGRESSION471 reports
ANAEMIA458 reports
METASTASES TO LIVER444 reports
SOMNOLENCE443 reports
DEPRESSION421 reports
PNEUMONIA407 reports
BLOOD PRESSURE INCREASED398 reports
DRUG INTERACTION388 reports
BREAST CANCER METASTATIC382 reports
GAIT DISTURBANCE381 reports
VISION BLURRED378 reports
CHILLS367 reports
NEOPLASM PROGRESSION366 reports
NEUROPATHY PERIPHERAL364 reports
ABDOMINAL DISCOMFORT352 reports
FEELING ABNORMAL350 reports
ASCITES342 reports
METASTASES TO LUNG340 reports
CONDITION AGGRAVATED338 reports
PERIPHERAL SWELLING330 reports
DRY SKIN325 reports
HAIR TEXTURE ABNORMAL324 reports
HYPERTENSION323 reports
COVID 19320 reports
SYNCOPE314 reports
HAIR COLOUR CHANGES312 reports
TACHYCARDIA309 reports
WEIGHT INCREASED307 reports
EYE PAIN306 reports
PLATELET COUNT DECREASED304 reports
URINARY TRACT INFECTION298 reports
MEMORY IMPAIRMENT297 reports
NASOPHARYNGITIS297 reports
MADAROSIS292 reports
HAEMOGLOBIN DECREASED289 reports
SEPSIS289 reports
CHEST PAIN286 reports
MUSCLE SPASMS283 reports
HAIR DISORDER280 reports
PRODUCT DOSE OMISSION ISSUE280 reports
HEAD DISCOMFORT277 reports
DRUG INTOLERANCE276 reports
PARAESTHESIA273 reports
BLINDNESS267 reports
HYPERSENSITIVITY266 reports
LEUKOPENIA258 reports
TINNITUS257 reports
HYPOAESTHESIA255 reports
THROMBOCYTOPENIA247 reports
HAEMATEMESIS241 reports
DEHYDRATION240 reports
HAEMORRHAGIC STROKE240 reports
DIPLOPIA239 reports
COMA236 reports
OCULAR DISCOMFORT236 reports
PRESYNCOPE235 reports
ERYTHEMA234 reports
VISUAL IMPAIRMENT234 reports
ALTERED STATE OF CONSCIOUSNESS233 reports
STOMATITIS231 reports
CARDIO RESPIRATORY ARREST230 reports
PRODUCT USE ISSUE223 reports
ACUTE KIDNEY INJURY222 reports

Report Outcomes

Out of 20,061 classified reports for ANASTROZOLE TABLETS:

Serious 73.2%Non-Serious 26.8%

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

Demographics Breakdown

Reports by Sex

Female17,022 (93.1%)
Male1,183 (6.5%)
Unknown83 (0.5%)

Reports by Age

Age 63533 reports
Age 69500 reports
Age 62485 reports
Age 60434 reports
Age 61422 reports
Age 65421 reports
Age 70393 reports
Age 58390 reports
Age 68390 reports
Age 67388 reports
Age 72383 reports
Age 66382 reports
Age 75381 reports
Age 57370 reports
Age 64368 reports
Age 73359 reports
Age 56353 reports
Age 71344 reports
Age 74340 reports
Age 76334 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with ANASTROZOLE TABLETS?

This profile reflects 50,885 FDA FAERS reports that mention ANASTROZOLE TABLETS. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for ANASTROZOLE TABLETS?

Frequently reported terms in FAERS include FATIGUE, NAUSEA, DIARRHOEA, ARTHRALGIA, ALOPECIA, HEADACHE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures ANASTROZOLE TABLETS?

Labeling and FAERS entries often list Avet Pharmaceuticals Inc in connection with ANASTROZOLE TABLETS. Always verify the specific product and NDC with your pharmacist.

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.