DRONABINOL

N/A

Manufactured by ThePharmaNetwork, LLC

17,794 FDA adverse event reports analyzed

Last updated: 2026-04-14

About DRONABINOL

DRONABINOL is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ThePharmaNetwork, LLC. The most commonly reported adverse reactions for DRONABINOL include NAUSEA, FATIGUE, DIARRHOEA, DEATH, VOMITING. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for DRONABINOL.

Top Adverse Reactions

NAUSEA879 reports
FATIGUE697 reports
DIARRHOEA604 reports
DEATH593 reports
VOMITING582 reports
OFF LABEL USE490 reports
DECREASED APPETITE446 reports
PAIN427 reports
WEIGHT DECREASED414 reports
DYSPNOEA377 reports
ASTHENIA375 reports
DRUG INEFFECTIVE319 reports
TOXICITY TO VARIOUS AGENTS314 reports
HEADACHE311 reports
PNEUMONIA302 reports
DRUG ABUSE282 reports
DEHYDRATION281 reports
DIZZINESS259 reports
ANXIETY256 reports
PYREXIA235 reports
FALL228 reports
ABDOMINAL PAIN226 reports
CONSTIPATION217 reports
BACK PAIN216 reports
RASH195 reports
INSOMNIA194 reports
DEPRESSION192 reports
MALAISE192 reports
URINARY TRACT INFECTION186 reports
ANAEMIA181 reports
CONFUSIONAL STATE180 reports
SEPSIS175 reports
DISEASE PROGRESSION164 reports
SOMNOLENCE163 reports
HYPOTENSION159 reports
PAIN IN EXTREMITY158 reports
ARTHRALGIA156 reports
DRUG SCREEN POSITIVE154 reports
ABDOMINAL PAIN UPPER142 reports
COUGH139 reports
MALIGNANT NEOPLASM PROGRESSION139 reports
CONDITION AGGRAVATED137 reports
THROMBOCYTOPENIA134 reports
FEELING ABNORMAL133 reports
ACUTE KIDNEY INJURY131 reports
OVERDOSE131 reports
GAIT DISTURBANCE129 reports
DRUG INTERACTION128 reports
COVID 19120 reports
PLEURAL EFFUSION120 reports
PLATELET COUNT DECREASED119 reports
WHITE BLOOD CELL COUNT DECREASED117 reports
RENAL FAILURE116 reports
EMOTIONAL DISTRESS113 reports
HAEMOGLOBIN DECREASED113 reports
NEUTROPENIA106 reports
CHEST PAIN104 reports
FEBRILE NEUTROPENIA104 reports
PRODUCT USE IN UNAPPROVED INDICATION102 reports
WEIGHT INCREASED101 reports
CHRONIC KIDNEY DISEASE100 reports
HYPERTENSION100 reports
MUSCLE SPASMS100 reports
OEDEMA PERIPHERAL100 reports
PRURITUS98 reports
DRUG DEPENDENCE97 reports
PRODUCT DOSE OMISSION ISSUE96 reports
INFECTION94 reports
POISONING94 reports
ANHEDONIA92 reports
TREMOR92 reports
BRAIN OEDEMA91 reports
HYPOKALAEMIA90 reports
SEIZURE88 reports
AGITATION87 reports
BLOOD PRESSURE INCREASED86 reports
PULMONARY OEDEMA85 reports
AGGRESSION82 reports
ALOPECIA82 reports
GENERAL PHYSICAL HEALTH DETERIORATION82 reports
DYSPHAGIA81 reports
HYPOAESTHESIA81 reports
NEUROPATHY PERIPHERAL81 reports
MEMORY IMPAIRMENT78 reports
NASOPHARYNGITIS78 reports
OSTEOPOROSIS78 reports
ABDOMINAL DISCOMFORT77 reports
PULMONARY EMBOLISM77 reports
STOMATITIS76 reports
CHILLS74 reports
DEEP VEIN THROMBOSIS74 reports
PANCYTOPENIA74 reports
RESPIRATORY FAILURE74 reports
SYNCOPE73 reports
CARDIO RESPIRATORY ARREST72 reports
HEART RATE INCREASED71 reports
MUSCULAR WEAKNESS71 reports
PERIPHERAL SWELLING71 reports
ABDOMINAL DISTENSION70 reports
HOSPITALISATION70 reports

Report Outcomes

Out of 7,815 classified reports for DRONABINOL:

Serious 75.0%Non-Serious 25.0%

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

Male3,812 (51.7%)
Female3,557 (48.2%)
Unknown7 (0.1%)

Reports by Age

Age 65150 reports
Age 64137 reports
Age 66132 reports
Age 61121 reports
Age 58120 reports
Age 67110 reports
Age 56105 reports
Age 62105 reports
Age 68101 reports
Age 75101 reports
Age 55100 reports
Age 4799 reports
Age 5097 reports
Age 4194 reports
Age 6094 reports
Age 5493 reports
Age 7092 reports
Age 6389 reports
Age 5388 reports
Age 6988 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 DRONABINOL?

This profile reflects 17,794 FDA FAERS reports that mention DRONABINOL. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for DRONABINOL?

Frequently reported terms in FAERS include NAUSEA, FATIGUE, DIARRHOEA, DEATH, VOMITING, OFF LABEL USE. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures DRONABINOL?

Labeling and FAERS entries often list ThePharmaNetwork, LLC in connection with DRONABINOL. 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.