Is GENERAL PHYSICAL HEALTH DETERIORATION a side effect of ZETIA ? ( FactMed.com )

About this FactMed analysis covering adverse side effect reports of ZETIA patients who developed GENERAL PHYSICAL HEALTH DETERIORATION.

FactMed provides MD-approved analysis to help both patients, researchers, and physicians accurately assess the risk profile for more than 20,000 different pharmaceutical products. The below report offers compiled information from Food & Drug Administration and FactMed user submissions. Between January 2004 and October 2012, 94 individuals taking ZETIA reported GENERAL PHYSICAL HEALTH DETERIORATION to the FDA. A total of 21297 ZETIA drug adverse event reaction reports were made with the FDA during this time period. Often the FDA only receives reports of the most critical and severe cases; these numbers may therefore underrepresent the complication rate of the medication.

FDA Research Report

Introduction This page is designed to help you determine the relationship, if any, between ZETIA and GENERAL PHYSICAL HEALTH DETERIORATION. In doing so, we compare ZETIA with other drugs that cause GENERAL PHYSICAL HEALTH DETERIORATION, to help you evaluate whether or not ZETIA causes GENERAL PHYSICAL HEALTH DETERIORATION. Likewise, this page shows the most highly-reported side effects of ZETIA, so you can see if GENERAL PHYSICAL HEALTH DETERIORATION ranks among ZETIA's most well-known side effects.

Summary Statistics
Reports of ZETIA causing GENERAL PHYSICAL HEALTH DETERIORATION: 94
Reports of any side effect of ZETIA : 21297
Percentage of ZETIA patients where GENERAL PHYSICAL HEALTH DETERIORATION is a reported side effect: 0.4414%

FDA reports of any drug causing GENERAL PHYSICAL HEALTH DETERIORATION : 32389
Average percentage for all medicated patients where GENERAL PHYSICAL HEALTH DETERIORATION is reported as a complication: 0.2030%

Physician opinion on ZETIA as adverse event culprit:

Overall opinion for all reports of this drug:

Most frequent diagnoses/indications for prescribing ZETIA:

BLOOD CHOLESTEROL INCREASED ( 3041 patients )
HYPERCHOLESTEROLAEMIA ( 1797 patients )
HYPERLIPIDAEMIA ( 943 patients )
PRODUCT USED FOR UNKNOWN INDICATION ( 866 patients )
BLOOD CHOLESTEROL ( 570 patients )
DRUG USE FOR UNKNOWN INDICATION ( 510 patients )
DYSLIPIDAEMIA ( 266 patients )
BLOOD CHOLESTEROL ABNORMAL ( 116 patients )
TYPE IIA HYPERLIPIDAEMIA ( 102 patients )
LOW DENSITY LIPOPROTEIN INCREASED ( 98 patients )
BLOOD TRIGLYCERIDES INCREASED ( 76 patients )
CARDIAC DISORDER ( 69 patients )
CORONARY ARTERY DISEASE ( 67 patients )
LIPIDS INCREASED ( 57 patients )
HYPERTENSION ( 39 patients )
HYPERTRIGLYCERIDAEMIA ( 29 patients )
METABOLIC DISORDER ( 21 patients )
LIPIDS ABNORMAL ( 21 patients )
ILL-DEFINED DISORDER ( 19 patients )
DIABETES MELLITUS ( 14 patients )
BLOOD CHOLESTEROL DECREASED ( 13 patients )
PROPHYLAXIS ( 13 patients )
MIXED HYPERLIPIDAEMIA ( 12 patients )
HIGH DENSITY LIPOPROTEIN DECREASED ( 11 patients )
LIPID METABOLISM DISORDER ( 11 patients )
LIPIDS ( 10 patients )
MYOCARDIAL ISCHAEMIA ( 9 patients )
LOW DENSITY LIPOPROTEIN ( 9 patients )
ARTERIOSCLEROSIS ( 9 patients )
BLOOD PRESSURE ( 8 patients )
TYPE II HYPERLIPIDAEMIA ( 8 patients )
TACHYCARDIA ( 8 patients )
HIGH DENSITY LIPOPROTEIN INCREASED ( 5 patients )
BLOOD TRIGLYCERIDES ABNORMAL ( 5 patients )
CARDIOVASCULAR EVENT PROPHYLAXIS ( 5 patients )
BLOOD TRIGLYCERIDES ( 5 patients )
TYPE 2 DIABETES MELLITUS ( 5 patients )
LOW DENSITY LIPOPROTEIN DECREASED ( 4 patients )
MYOCARDIAL INFARCTION ( 4 patients )
DYSPEPSIA ( 4 patients )
HEPATIC STEATOSIS ( 4 patients )
HYPERCHLORAEMIA ( 3 patients )
ACUTE MYOCARDIAL INFARCTION ( 3 patients )
LIVER FUNCTION TEST ABNORMAL ( 3 patients )
HYPOCHOLESTEROLAEMIA ( 3 patients )
LDL/HDL RATIO ( 3 patients )
DRUG INTOLERANCE ( 3 patients )
CEREBROVASCULAR ACCIDENT ( 3 patients )
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 patients )
CEREBRAL ARTERIOSCLEROSIS ( 2 patients )
CEREBROVASCULAR ACCIDENT PROPHYLAXIS ( 2 patients )
PERIPHERAL VASCULAR DISORDER ( 2 patients )
GASTRIC DISORDER ( 2 patients )
AORTIC ARTERIOSCLEROSIS ( 2 patients )
CORONARY ARTERY OCCLUSION ( 2 patients )
HEART VALVE INCOMPETENCE ( 2 patients )
INSOMNIA ( 2 patients )
CHEST PAIN ( 2 patients )
BLOOD GLUCOSE ( 2 patients )
COLITIS ( 2 patients )
BLOOD PRESSURE ABNORMAL ( 2 patients )
HYPO HDL CHOLESTEROLAEMIA ( 2 patients )
ARTERIAL OCCLUSIVE DISEASE ( 2 patients )
DEPRESSION ( 2 patients )
CARDIOVASCULAR DISORDER ( 2 patients )
DRUG THERAPY ( 1 patients )
OSTEOARTHRITIS ( 1 patients )
BLOOD DISORDER ( 1 patients )
LIPIDS DECREASED ( 1 patients )
WEIGHT CONTROL ( 1 patients )
CHRONIC MYELOID LEUKAEMIA ( 1 patients )
ELDER ABUSE ( 1 patients )
LIPOPROTEIN (A) ABNORMAL ( 1 patients )
CORONARY ARTERIAL STENT INSERTION ( 1 patients )
BLOOD PRESSURE INCREASED ( 1 patients )
PSYCHOMOTOR HYPERACTIVITY ( 1 patients )
HEART TRANSPLANT ( 1 patients )
ARTERIAL STENOSIS ( 1 patients )
CRIME ( 1 patients )
STENT PLACEMENT ( 1 patients )
ATHEROSCLEROSIS ( 1 patients )
THERAPEUTIC PROCEDURE ( 1 patients )
CARDIAC STRESS TEST ABNORMAL ( 1 patients )
HEPATITIS ( 1 patients )
MUSCLE SPASMS ( 1 patients )
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 patients )
DRUG HYPERSENSITIVITY ( 1 patients )
TRANSIENT ISCHAEMIC ATTACK ( 1 patients )
HYPERBILIRUBINAEMIA ( 1 patients )
NEPHROTIC SYNDROME ( 1 patients )
VASOSPASM ( 1 patients )
PAIN ( 1 patients )
XANTHELASMA ( 1 patients )
ACUTE CORONARY SYNDROME ( 1 patients )
FAMILIAL RISK FACTOR ( 1 patients )
LIPOPROTEIN (A) INCREASED ( 1 patients )
ANXIETY ( 1 patients )
PROPHYLAXIS AGAINST TRANSPLANT REJECTION ( 1 patients )
GLUCOSE TOLERANCE IMPAIRED ( 1 patients )
CORONARY ARTERY SURGERY ( 1 patients )
HYPOLIPIDAEMIA ( 1 patients )
RHEUMATOID ARTHRITIS ( 1 patients )
HEART VALVE CALCIFICATION ( 1 patients )
INFECTION ( 1 patients )
CARDIAC OPERATION ( 1 patients )
ATHEROSCLEROSIS PROPHYLAXIS ( 1 patients )
LABORATORY TEST ABNORMAL ( 1 patients )
THROMBOLYSIS ( 1 patients )
HEPATOCELLULAR INJURY ( 1 patients )
MYALGIA ( 1 patients )
DRUG INEFFECTIVE ( 1 patients )
LDL/HDL RATIO INCREASED ( 1 patients )
( 0 patients )

Drugs with high FDA adverse event association with GENERAL PHYSICAL HEALTH DETERIORATION:

ZOMETA (3877 patients)
YAZ (2956 patients)
YASMIN (2798 patients)
ASPIRIN (2358 patients)
MAGNEVIST (2354 patients)
AREDIA (1658 patients)
OMNISCAN (1481 patients)
PREDNISONE (1433 patients)
LASIX (1360 patients)
FUROSEMIDE (1323 patients)
OMEPRAZOLE (1274 patients)
DEXAMETHASONE (1268 patients)
DROSPIRENONE AND ETHINYL ESTRADIOL (1222 patients)
NEXIUM (1174 patients)
ACETAMINOPHEN (1161 patients)
PREDNISOLONE (1081 patients)
OPTIMARK (994 patients)
METHOTREXATE (926 patients)
LISINOPRIL (900 patients)
HUMIRA (888 patients)
NEURONTIN (872 patients)
SIMVASTATIN (872 patients)
COUMADIN (872 patients)
ALLOPURINOL (866 patients)
LIPITOR (863 patients)
OXYCONTIN (846 patients)
IBUPROFEN (837 patients)
LEVOTHYROXINE SODIUM (837 patients)
PROHANCE (819 patients)
MULTIHANCE (815 patients)
LORAZEPAM (815 patients)
CISPLATIN (759 patients)
FOLIC ACID (753 patients)
FLUOROURACIL (734 patients)
PRILOSEC (728 patients)
DIGOXIN (719 patients)
CYCLOPHOSPHAMIDE (712 patients)
AMBIEN (702 patients)
ATENOLOL (694 patients)
PLAVIX (694 patients)
REVLIMID (677 patients)
LYRICA (675 patients)
POTASSIUM CHLORIDE (675 patients)
MORPHINE (674 patients)
ZOLOFT (655 patients)
ATIVAN (655 patients)
PROTONIX (645 patients)
PERCOCET (643 patients)
XANAX (634 patients)
VELCADE (620 patients)
AMOXICILLIN (612 patients)
ZOFRAN (608 patients)
AVASTIN (602 patients)
DECADRON (593 patients)
FORTEO (590 patients)
PREDNISONE TAB (589 patients)
RAMIPRIL (588 patients)
ALBUTEROL (587 patients)
OXYCODONE HCL (583 patients)
EFFEXOR (573 patients)
SYNTHROID (571 patients)
XELODA (571 patients)
VICODIN (571 patients)
GABAPENTIN (559 patients)
NORVASC (549 patients)
MORPHINE SULFATE (543 patients)
METFORMIN HCL (543 patients)
TAXOTERE (534 patients)
WARFARIN SODIUM (530 patients)
CELEBREX (529 patients)
METOPROLOL TARTRATE (528 patients)
CAPECITABINE (527 patients)
HEPARIN SODIUM INJECTION (524 patients)
SPIRONOLACTONE (515 patients)
CIPROFLOXACIN (505 patients)
VIOXX (502 patients)
CLOZARIL (499 patients)
FENTANYL (498 patients)
HYDROCHLOROTHIAZIDE (494 patients)
CHEMOTHERAPEUTICS NOS (491 patients)
VANCOMYCIN (490 patients)
ARANESP (489 patients)
TYSABRI (488 patients)
DURAGESIC-100 (477 patients)
EPOGEN (475 patients)
CARBOPLATIN (475 patients)
TOPROL-XL (468 patients)
ZOCOR (464 patients)
ZYPREXA (458 patients)
AMLODIPINE (451 patients)
FOSAMAX (447 patients)
FEMARA (444 patients)
COMPAZINE (438 patients)
LEVAQUIN (438 patients)
VITAMIN D (438 patients)
PANTOPRAZOLE (427 patients)
TRAMADOL HCL (425 patients)
LEXAPRO (420 patients)
LANTUS (417 patients)
CALCIUM (412 patients)
GADOLINIUM IN UNSPECIFIED DRUG (411 patients)
SEROQUEL (411 patients)
PREVACID (406 patients)
BACTRIM (406 patients)
INSULIN (405 patients)
SANDOSTATIN LAR (402 patients)
DIOVAN (401 patients)
BISOPROLOL FUMARATE (401 patients)
OXALIPLATIN (397 patients)
THALIDOMIDE (395 patients)
BEVACIZUMAB (387 patients)
FLUCONAZOLE (384 patients)
ADVAIR DISKUS 100/50 (382 patients)
REMICADE (382 patients)
PANTOPRAZOLE SODIUM (378 patients)
VINCRISTINE (378 patients)
HEPARIN (378 patients)
MULTI-VITAMINS (373 patients)
LOVENOX (369 patients)
LORTAB (369 patients)
PACLITAXEL (368 patients)
TAXOL (366 patients)
GLEEVEC (366 patients)
METOCLOPRAMIDE (366 patients)
VITAMIN B-12 (365 patients)
RENAGEL (364 patients)
LANSOPRAZOLE (364 patients)
SORAFENIB (361 patients)
ALDACTONE (360 patients)
ACYCLOVIR (356 patients)
AUGMENTIN '125' (354 patients)
RADIATION THERAPY (352 patients)
PAXIL (350 patients)
GEMZAR (350 patients)
ALPRAZOLAM (348 patients)
FERROUS SULFATE TAB (347 patients)
LACTULOSE (347 patients)
RISPERDAL (345 patients)
TAMOXIFEN CITRATE (345 patients)
CYMBALTA (338 patients)
SPIRIVA (338 patients)
COREG (335 patients)
DOXORUBICIN HCL (335 patients)
PROGRAF (333 patients)
CITALOPRAM HYDROBROMIDE (332 patients)
DILAUDID (332 patients)
CLONAZEPAM (332 patients)
NITROGLYCERIN (329 patients)
CALCIUM CARBONATE (329 patients)
RITUXIMAB (327 patients)
ENALAPRIL MALEATE (326 patients)
REGLAN (322 patients)
SUTENT (314 patients)
METRONIDAZOLE (312 patients)
DOCETAXEL (311 patients)
SOLU-MEDROL (310 patients)
TORSEMIDE (309 patients)
METHYLPREDNISOLONE (307 patients)
CLINDAMYCIN (305 patients)
MS CONTIN (304 patients)
WELLBUTRIN (303 patients)
EXJADE (299 patients)
HALDOL (298 patients)
CELEXA (298 patients)
MOTRIN (295 patients)
CLOZAPINE (295 patients)
FASLODEX (293 patients)
KEPPRA (292 patients)
AFINITOR (290 patients)
DIAZEPAM (290 patients)
MIRTAZAPINE (288 patients)
CYTARABINE (288 patients)
AVONEX (287 patients)
CLONIDINE (285 patients)
CRESTOR (281 patients)
ALTACE (278 patients)
ARIMIDEX (275 patients)
EXELON (274 patients)
CORDARONE (274 patients)
GLUCOPHAGE (273 patients)
DIFLUCAN (273 patients)
ENBREL (273 patients)
ZITHROMAX (271 patients)
DEXAMETHASONE TAB (270 patients)
AMITRIPTYLINE HCL (268 patients)
ROCEPHIN (266 patients)
CELLCEPT (265 patients)
HYDROCORTISONE (264 patients)
NEUPOGEN (263 patients)
LOPRESSOR (257 patients)
METOPROLOL SUCCINATE (256 patients)
AVANDIA (255 patients)
CYCLOSPORINE (255 patients)
KALETRA (254 patients)
TEMAZEPAM (254 patients)
RANITIDINE (252 patients)
ZANTAC (251 patients)
AZITHROMYCIN (251 patients)
PERIDEX (250 patients)
FLEXERIL (250 patients)
ZYRTEC (248 patients)
FAMOTIDINE (245 patients)
ZOLPIDEM (245 patients)
FLAGYL (244 patients)
PROZAC (243 patients)
ONDANSETRON (242 patients)
AMIODARONE HCL (240 patients)
KLONOPIN (238 patients)
ENOXAPARIN SODIUM (238 patients)
TRAZODONE HCL (237 patients)

Most common side effects for patients taking ZETIA:

MYALGIA (1541 patients)
NAUSEA (1461 patients)
FATIGUE (1293 patients)
DIZZINESS (1224 patients)
PAIN (1161 patients)
DYSPNOEA (1108 patients)
ASTHENIA (1059 patients)
PAIN IN EXTREMITY (1026 patients)
DRUG INEFFECTIVE (938 patients)
ARTHRALGIA (913 patients)
HEADACHE (858 patients)
MYOCARDIAL INFARCTION (819 patients)
DIARRHOEA (814 patients)
FALL (759 patients)
BACK PAIN (755 patients)
ANXIETY (740 patients)
CHEST PAIN (704 patients)
OEDEMA PERIPHERAL (697 patients)
DEPRESSION (688 patients)
VOMITING (681 patients)
WEIGHT DECREASED (647 patients)
BLOOD GLUCOSE INCREASED (642 patients)
ABDOMINAL PAIN (640 patients)
BLOOD CREATINE PHOSPHOKINASE INCREASED (628 patients)
FLUSHING (605 patients)
PRURITUS (603 patients)
MUSCLE SPASMS (570 patients)
MUSCULAR WEAKNESS (550 patients)
HYPERTENSION (534 patients)
INSOMNIA (524 patients)
CONSTIPATION (519 patients)
RASH (514 patients)
MALAISE (514 patients)
ANAEMIA (491 patients)
CARDIAC FAILURE CONGESTIVE (488 patients)
RHABDOMYOLYSIS (481 patients)
RENAL FAILURE (478 patients)
INJURY (473 patients)
BLOOD CHOLESTEROL INCREASED (467 patients)
PNEUMONIA (450 patients)
WEIGHT INCREASED (448 patients)
PYREXIA (439 patients)
GAIT DISTURBANCE (435 patients)
RENAL FAILURE ACUTE (427 patients)
CORONARY ARTERY DISEASE (426 patients)
HYPOTENSION (424 patients)
PARAESTHESIA (410 patients)
ATRIAL FIBRILLATION (405 patients)
FEELING ABNORMAL (403 patients)
ABDOMINAL PAIN UPPER (397 patients)
COUGH (395 patients)
URINARY TRACT INFECTION (377 patients)
CEREBROVASCULAR ACCIDENT (372 patients)
ALANINE AMINOTRANSFERASE INCREASED (372 patients)
HYPOAESTHESIA (365 patients)
ASPARTATE AMINOTRANSFERASE INCREASED (355 patients)
SOMNOLENCE (348 patients)
PANCREATITIS (344 patients)
DECREASED APPETITE (330 patients)
HEPATIC ENZYME INCREASED (317 patients)
LIVER FUNCTION TEST ABNORMAL (316 patients)
DIABETES MELLITUS (316 patients)
DEHYDRATION (315 patients)
GASTROOESOPHAGEAL REFLUX DISEASE (314 patients)
DRUG INTERACTION (313 patients)
PALPITATIONS (307 patients)
DYSPEPSIA (296 patients)
TREMOR (295 patients)
VISION BLURRED (294 patients)
BLOOD PRESSURE INCREASED (293 patients)
ERYTHEMA (290 patients)
CONFUSIONAL STATE (289 patients)
HYPERHIDROSIS (289 patients)
DEATH (283 patients)
BLOOD CREATININE INCREASED (263 patients)
SYNCOPE (262 patients)
EMOTIONAL DISTRESS (258 patients)
DYSPHAGIA (257 patients)
CHEST DISCOMFORT (256 patients)
ABDOMINAL DISTENSION (254 patients)
HYPERSENSITIVITY (252 patients)
CARDIAC DISORDER (251 patients)
HYPERLIPIDAEMIA (246 patients)
ABDOMINAL DISCOMFORT (243 patients)
ALOPECIA (241 patients)
LOSS OF CONSCIOUSNESS (241 patients)
NEUROPATHY PERIPHERAL (229 patients)
CONDITION AGGRAVATED (229 patients)
JOINT SWELLING (224 patients)
FEELING HOT (221 patients)
BLOOD TRIGLYCERIDES INCREASED (219 patients)
OSTEOARTHRITIS (218 patients)
URTICARIA (216 patients)
ANHEDONIA (216 patients)
SWELLING (216 patients)
CONTUSION (212 patients)
AMNESIA (212 patients)
DRY MOUTH (211 patients)
CHOLELITHIASIS (209 patients)
FLATULENCE (209 patients)
ANGINA PECTORIS (206 patients)
MUSCULOSKELETAL PAIN (204 patients)
UNEVALUABLE EVENT (195 patients)
BURNING SENSATION (194 patients)
HYPOGLYCAEMIA (192 patients)
INFECTION (192 patients)
CONVULSION (191 patients)
OSTEONECROSIS OF JAW (190 patients)
MUSCULOSKELETAL STIFFNESS (190 patients)
MEMORY IMPAIRMENT (186 patients)
PANCREATITIS ACUTE (184 patients)
BLOOD GLUCOSE DECREASED (184 patients)
BRONCHITIS (181 patients)
CHILLS (181 patients)
DYSURIA (180 patients)
HAEMOGLOBIN DECREASED (180 patients)
DYSGEUSIA (180 patients)
INTERNATIONAL NORMALISED RATIO INCREASED (176 patients)
BALANCE DISORDER (176 patients)
HEART RATE INCREASED (175 patients)
RENAL IMPAIRMENT (173 patients)
RESPIRATORY FAILURE (170 patients)
PAIN IN JAW (168 patients)
TRANSIENT ISCHAEMIC ATTACK (168 patients)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (167 patients)
PLEURAL EFFUSION (164 patients)
ECONOMIC PROBLEM (161 patients)
SPINAL OSTEOARTHRITIS (160 patients)
ADVERSE EVENT (159 patients)
ARTERIOSCLEROSIS (159 patients)
HYPERGLYCAEMIA (159 patients)
LOW DENSITY LIPOPROTEIN INCREASED (158 patients)
HAEMORRHAGE (157 patients)
BONE DISORDER (157 patients)
LIVER DISORDER (156 patients)
NECK PAIN (155 patients)
SINUSITIS (155 patients)
CORONARY ARTERY OCCLUSION (154 patients)
THROMBOCYTOPENIA (154 patients)
MYOPATHY (153 patients)
DEEP VEIN THROMBOSIS (153 patients)
ABASIA (152 patients)
STRESS (151 patients)
TYPE 2 DIABETES MELLITUS (151 patients)
ARTHRITIS (151 patients)
SWELLING FACE (148 patients)
OSTEONECROSIS (148 patients)
OVERDOSE (147 patients)
OEDEMA (145 patients)
EPISTAXIS (145 patients)
CARDIAC FAILURE (143 patients)
DYSPHONIA (142 patients)
NEPHROLITHIASIS (142 patients)
MENTAL STATUS CHANGES (141 patients)
MITRAL VALVE INCOMPETENCE (141 patients)
RENAL FAILURE CHRONIC (141 patients)
CARDIAC ARREST (140 patients)
OSTEOMYELITIS (138 patients)
ATELECTASIS (138 patients)
PHARMACEUTICAL PRODUCT COMPLAINT (138 patients)
OSTEOPOROSIS (137 patients)
ARRHYTHMIA (137 patients)
SEPSIS (136 patients)
ACUTE MYOCARDIAL INFARCTION (136 patients)
MEDICATION ERROR (136 patients)
CELLULITIS (136 patients)
HOT FLUSH (136 patients)
BLOOD PRESSURE DECREASED (136 patients)
INJECTION SITE PAIN (134 patients)
GASTROINTESTINAL HAEMORRHAGE (134 patients)
TACHYCARDIA (133 patients)
DRUG HYPERSENSITIVITY (132 patients)
BLOOD ALKALINE PHOSPHATASE INCREASED (131 patients)
HEPATIC STEATOSIS (131 patients)
SLEEP APNOEA SYNDROME (130 patients)
FEAR (128 patients)
ASTHMA (127 patients)
MULTI-ORGAN FAILURE (124 patients)
ARTHROPATHY (122 patients)
OFF LABEL USE (121 patients)
OSTEOPENIA (120 patients)
INTERVERTEBRAL DISC DEGENERATION (120 patients)
VISUAL ACUITY REDUCED (118 patients)
BONE PAIN (117 patients)
BRADYCARDIA (117 patients)
INTERVERTEBRAL DISC PROTRUSION (116 patients)
MYOCARDIAL ISCHAEMIA (114 patients)
GASTRITIS (114 patients)
DIVERTICULUM (112 patients)
HALLUCINATION (111 patients)
SLEEP DISORDER (110 patients)
INFLUENZA LIKE ILLNESS (110 patients)
HAEMORRHOIDS (109 patients)
MUSCLE DISORDER (108 patients)
SUICIDAL IDEATION (107 patients)
HYPERCHOLESTEROLAEMIA (107 patients)
BLOOD UREA INCREASED (107 patients)
WRONG TECHNIQUE IN DRUG USAGE PROCESS (107 patients)
PULMONARY EMBOLISM (107 patients)
HEPATITIS (107 patients)
RHINORRHOEA (105 patients)
DYSPNOEA EXERTIONAL (105 patients)
SWOLLEN TONGUE (105 patients)
ANOREXIA (105 patients)
RASH PRURITIC (103 patients)
RIB FRACTURE (103 patients)
LETHARGY (103 patients)
PLATELET COUNT DECREASED (103 patients)
DISORIENTATION (103 patients)
ERECTILE DYSFUNCTION (102 patients)

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Recent FactMed Activity for ZETIA

Issue	Description / Topic	Timestamp
QUESTION MYASTHENIA GRAVIS	I have myasthenia gravis 70yr old,also diabetes/HTN high cholesterol - (hx ca prostate/bladder in remission post chemo/radiation). want to start Zetia but have had terrible results with Lipitor other statin drugs leading to chewing/slurred speech problems. Now on q6wk IVIG treatments and symptoms appear to be subsiding. What is a possible med for the cholesterol??	2015-01-20 15:32:53
QUESTION PLATELET COUNT INCREASED	I have been on zetia for 6 months..blood work today showed platelet count at 730..no previous problems with plt count...wondering could zetia be causing this increase?	2015-02-09 17:04:30
QUESTION FOOD INTERACTION	Can you east citrus products when taking Zetia? Many warnings exists about taking cholesterol medications and citrus products such as grapefruit and oranges.	2015-02-10 19:35:30
QUESTION CELLULITIS STREPTOCOCCAL	I have been on Zetia for one week and have been diagnosed with unexplained staphylococcus cellulitis. Could Zetia be the cause?	2015-03-10 09:09:25
QUESTION CELLULITIS STREPTOCOCCAL	I have been on Zetia for one week and have been diagnosed with unexplained staphylococcus cellulitis. Could Zetia be the cause?	2015-03-10 09:11:57
QUESTION HOARSENESS	Is hoarseness usually a temporary side effect when beginning to take the drug Zetia?	2015-05-21 08:50:44
QUESTION LYMPHOMA	I have non Hoskins lymphoma, should I take zetia?	2015-06-16 09:20:29
QUESTION WHITE BLOOD CELL COUNT	can Zetia cause low white blood count	2015-06-22 15:26:08
QUESTION ACNE	I'm female, 71yrs. Taking Zetia. During the first 2 week I had a severe acne, and although reduce my cholesterol level I stopped for 2 weeks and the acne disappeared. I began again and the acne came again. Also I suffered back and whole body pain. I decided to stop all medication for cholesterol and began a vegan diet. I want to know how I can lower my levels without medication?	2015-12-19 08:54:13
QUESTION DRY MOUTH	Will dry mouth go away after taking zetia for a period of time	2016-01-16 18:18:56
QUESTION DRY MOUTH	Will dry mouth go away after taking zetia for a period of time	2016-01-16 18:22:43
QUESTION DRY MOUTH	Will dry mouth go away after taking zetia for a period of time	2016-01-16 20:29:36
QUESTION LOOSE STOOLS	Have been taking Zetia for three weeks now. Have morning lower back pain and loose stools. Is this common?	2016-01-23 12:39:41
QUESTION PANCYTOPENIA	Can zetia cause pancytopenia?	2016-03-05 19:22:27
QUESTION ARTHRITIS	Any connection between zetia and any form of arthritis?	2016-03-26 10:14:11
QUESTION CHOLECYSTITIS	ZETIA CAUSED ACUTE GALLSTONES ATTACK MUSCLE ACHES FLU SWOLLEN GLANDS.6 MONTHS LATER US SHOWED NON ACUTE GALLSTONES PLUS FATTY LIVER.I DONT DRINK.HOW DO I PREVENT LIVER CA.HOW DO I REVERSE FATTY LIVER.JIM DOCSREC.COM	2016-04-01 08:55:41
CONCERN CHOLECYSTITIS	TY GP TOLD ME ZETIA HAD NO SE. HE GAVE ME SAMPLES.I TOOK 1 WITH LUNCH AND 1WITH DINNER.NEXT DAY 1 8AM PLUS 1 2PM. 4 IN 24HOURS,2 CONSECUTIVE DAYS. I GOT FLU SORE THROAT SWOLLEN GLANDS,MUSCLE ACHES,ABDOMINAL PAIN RU QUADRANT.I CALLED GP ASKED NURSE IF HE WOULD ORDER US OF GB. GP TOLD NURSE TO TELL ME TO STOP DIAGNOSING MYSELF.HE WOULD NOT ORDER US. I WAS BELCHING CONSTANTLY.I HAD VOMITED AFTER A FATTY MEAL THE NIGHT BEFORE.ITOOK1/4 CUP APPLE CIDER VINEGAR AND IT STOPPED BAD GALL BLADDER PAIN IN 20 NINUTES.IT KEPT FROM ER .A GI MD ORDERED US ABDOMEN . REPORT ACUTE GALLSTONES. GI MD ORDERED ACTIGAL WHICH HAS SIDE EFFECTS.INSTEAD I DID GB FLUSH WITH APPLE JUICE 4TBL EPSOM SAULT F/B 1/2CUP OLIVE OIL +GRAPEFRUIT. I FELT BETTER IN WEEKS.5MO LATER REPEAT US ABDOMIN SHOWS NON_ACUTE GALLSTONES PLUS NEW FATTY LIVER DISEASE.I STILL BELCH FREQUENTLY.IM NOW ON LOW FATLOW CARB DIET.I DONT DRINK. I KNOW ZETIA OD CAUSED ACUTE GALLSTONES AND FB FATTY LIVER. BAD DRUG. WHAT CAN CURE FATTY LIVER BEFORE I GET CANCER ?DOCSREC@MSN.COM.	2016-04-01 11:18:03
QUESTION IMMUNE SYSTEM DISORDER	Does Zetia cause Alopecia Areata	2016-06-18 19:26:24
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:44:40
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:44:41
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:44:51
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:44:51
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:44:54
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:01
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:07
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:13
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:22
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:22
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:23
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:29
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:29
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:29
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:32
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:33
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:37
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:37
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:38
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:39
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:55
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:45:59
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:00
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:01
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:01
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:01
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:11
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:11
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:12
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:17
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:20
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:20
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:28
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:29
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:33
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:33
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss	2016-07-17 08:46:35
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss2	2016-07-17 08:46:41
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss2	2016-07-17 08:46:43
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss2	2016-07-17 08:46:49
QUESTION BONE LOSS	Was on boniva until last bone test loss of 8%in hip only change started zetia can this be reason for bone loss2	2016-07-17 08:46:49
QUESTION TINNITUS	Can Zetia cause Tinnitis?	2017-03-14 16:36:41

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