About this FactMed analysis covering adverse side effect reports of ALMARL patients who developed DELIRIUM.

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, 7 individuals taking ALMARL reported DELIRIUM to the FDA. A total of 227 ALMARL 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 ALMARL and DELIRIUM. In doing so, we compare ALMARL with other drugs that cause DELIRIUM, to help you evaluate whether or not ALMARL causes DELIRIUM. Likewise, this page shows the most highly-reported side effects of ALMARL, so you can see if DELIRIUM ranks among ALMARL's most well-known side effects.
Summary Statistics
Reports of ALMARL causing DELIRIUM: 7
Reports of any side effect of ALMARL : 227
Percentage of ALMARL patients where DELIRIUM is a reported side effect: 3.0837%

FDA reports of any drug causing DELIRIUM : 11057
Average percentage for all medicated patients where DELIRIUM is reported as a complication: 0.0693%

Physician opinion on ALMARL as adverse event culprit:

Overall opinion for all reports of this drug:
Most frequent diagnoses/indications for prescribing ALMARL:
HYPERTENSION ( 76 patients )
PARKINSON'S DISEASE ( 8 patients )
ESSENTIAL TREMOR ( 6 patients )
ATRIAL FIBRILLATION ( 4 patients )
SCHIZOPHRENIA ( 2 patients )
TREMOR ( 2 patients )
ANGINA PECTORIS ( 2 patients )
DRUG USE FOR UNKNOWN INDICATION ( 2 patients )
PALPITATIONS ( 2 patients )
PRODUCT USED FOR UNKNOWN INDICATION ( 2 patients )
TACHYCARDIA ( 2 patients )
HYPERTROPHY ( 1 patients )
( 0 patients )
Drugs with high FDA adverse event association with DELIRIUM:

ASPIRIN (864 patients)
SEROQUEL (674 patients)
FOSAMAX (526 patients)
LORAZEPAM (519 patients)
HEPARIN SODIUM INJECTION (452 patients)
ACETAMINOPHEN (414 patients)
OXYCODONE HCL (387 patients)
LASIX (384 patients)
OMEPRAZOLE (360 patients)
VALTREX (358 patients)
TAMIFLU (354 patients)
ZYPREXA (353 patients)
OLANZAPINE (353 patients)
RISPERDAL (340 patients)
FUROSEMIDE (337 patients)
MORPHINE (333 patients)
CLONAZEPAM (318 patients)
SIMVASTATIN (303 patients)
LYRICA (302 patients)
VIOXX (294 patients)
OXYCONTIN (286 patients)
DIAZEPAM (286 patients)
PAXIL (278 patients)
HALOPERIDOL (273 patients)
CYMBALTA (268 patients)
CLOZAPINE (264 patients)
DIGOXIN (246 patients)
ALLOPURINOL (245 patients)
FENTANYL (241 patients)
TRAMADOL HCL (240 patients)
AMLODIPINE (239 patients)
NORVASC (239 patients)
REVLIMID (236 patients)
DEXAMETHASONE (232 patients)
CLOZARIL (231 patients)
MIRTAZAPINE (227 patients)
LIPITOR (222 patients)
LISINOPRIL (222 patients)
NEXIUM (220 patients)
LEVOTHYROXINE SODIUM (218 patients)
RELENZA (218 patients)
NEURONTIN (216 patients)
ZOLPIDEM (210 patients)
VALPROATE SODIUM (209 patients)
MYSLEE (207 patients)
BACLOFEN (206 patients)
AMITRIPTYLINE HCL (204 patients)
AMBIEN (200 patients)
PREDNISONE (200 patients)
FAMOTIDINE (198 patients)
PREDNISOLONE (195 patients)
DURAGESIC-100 (193 patients)
POTASSIUM CHLORIDE (191 patients)
WARFARIN SODIUM (190 patients)
GABAPENTIN (190 patients)
HALDOL (189 patients)
ATIVAN (188 patients)
PAROXETINE HCL (188 patients)
ATENOLOL (188 patients)
ARICEPT (182 patients)
XANAX (180 patients)
DUROTEP (178 patients)
LITHIUM CARBONATE (178 patients)
HYDROCHLOROTHIAZIDE (177 patients)
ALPRAZOLAM (175 patients)
ZOMETA (175 patients)
CITALOPRAM HYDROBROMIDE (172 patients)
EXELON (172 patients)
ZOLOFT (170 patients)
METOPROLOL TARTRATE (169 patients)
COUMADIN (169 patients)
MORPHINE SULFATE (168 patients)
ZOLPIDEM TARTRATE (165 patients)
FENTANYL-100 (164 patients)
TRAZODONE HCL (164 patients)
SYNTHROID (163 patients)
MAGNESIUM OXIDE (163 patients)
ACCUTANE (153 patients)
LEVOFLOXACIN (150 patients)
PLAVIX (148 patients)
PRILOSEC (146 patients)
RISPERIDONE (145 patients)
CIPROFLOXACIN (145 patients)
LEXAPRO (144 patients)
FLUCONAZOLE (140 patients)
FOLIC ACID (138 patients)
EFFEXOR (138 patients)
ZOCOR (133 patients)
LEPONEX (133 patients)
QUETIAPINE (133 patients)
DECADRON (133 patients)
INSULIN (132 patients)
METFORMIN HCL (132 patients)
LEVAQUIN (131 patients)
SERTRALINE HYDROCHLORIDE (131 patients)
PROTONIX (130 patients)
FLUOXETINE (130 patients)
LAMICTAL (129 patients)
DEPAKOTE (127 patients)
FENTANYL CITRATE (126 patients)
RIBAVIRIN (125 patients)
AVONEX (123 patients)
CLARITHROMYCIN (123 patients)
VICODIN (121 patients)
DIOVAN (120 patients)
LOXONIN (119 patients)
LANSOPRAZOLE (118 patients)
KEPPRA (116 patients)
CELEXA (116 patients)
CARBOPLATIN (116 patients)
METHOTREXATE (115 patients)
ZOVIRAX (115 patients)
TEGRETOL (113 patients)
NITROGLYCERIN (112 patients)
METOCLOPRAMIDE (110 patients)
REMICADE (110 patients)
ABILIFY (108 patients)
ALBUTEROL (108 patients)
RAMIPRIL (108 patients)
VOLTAREN (108 patients)
CALONAL (107 patients)
AKINETON (107 patients)
PROZAC (106 patients)
REQUIP (106 patients)
PERCOCET (103 patients)
CARBAMAZEPINE (103 patients)
ACYCLOVIR (102 patients)
QUETIAPINE FUMARATE (102 patients)
SINEMET (101 patients)
IBUPROFEN (101 patients)
PREVACID (100 patients)
PANTOPRAZOLE (100 patients)
PREDNISONE TAB (99 patients)
RANITIDINE (99 patients)
MUCODYNE (99 patients)
PANTOPRAZOLE SODIUM (99 patients)
PEG-INTRON (98 patients)
VANCOMYCIN (97 patients)
LENDORMIN (96 patients)
MORPHINE HYDROCHLORIDE (96 patients)
HYDROMORPHONE HCL (95 patients)
LANTUS (95 patients)
ZOFRAN (93 patients)
MUCOSTA (92 patients)
METOPROLOL (92 patients)
VITAMIN D (92 patients)
DEPAKENE (92 patients)
CLONIDINE (92 patients)
MULTI-VITAMIN (92 patients)
AREDIA (91 patients)
SPIRIVA (91 patients)
TEMAZEPAM (90 patients)
VELCADE (90 patients)
DUROTEP MT (90 patients)
LORTAB (89 patients)
TOPAMAX (88 patients)
PHENYTOIN (88 patients)
WELLBUTRIN (87 patients)
ZANTAC (87 patients)
PROGRAF (86 patients)
ENALAPRIL MALEATE (86 patients)
DEPAS (85 patients)
AVELOX (84 patients)
CELEBREX (83 patients)
METOPROLOL SUCCINATE (81 patients)
LOPRESSOR (81 patients)
KLONOPIN (81 patients)
CISPLATIN (80 patients)
DONEPEZIL HCL (79 patients)
VALPROIC ACID (78 patients)
TYLENOL (CAPLET) (77 patients)
LOVENOX (77 patients)
METRONIDAZOLE (77 patients)
REBETOL (77 patients)
ALDACTONE (77 patients)
ASVERIN (76 patients)
ISOSORBIDE DINITRATE (76 patients)
HEPARIN (76 patients)
RIVOTRIL (76 patients)
FLEXERIL (76 patients)
HUMIRA (75 patients)
REMERON (75 patients)
PREMARIN (75 patients)
EFFEXOR XR (75 patients)
RITALIN (74 patients)
STALEVO 100 (73 patients)
CYCLOSPORINE (73 patients)
PEGASYS (73 patients)
COLACE (72 patients)
DILAUDID (72 patients)
LACTULOSE (71 patients)
BUPROPION HCL (71 patients)
METHADONE HCL (71 patients)
SPIRONOLACTONE (71 patients)
FERROUS SULFATE TAB (71 patients)
CALCIUM (71 patients)
ZITHROMAX (71 patients)
CALCIUM CARBONATE (70 patients)
VENLAFAXINE HCL (70 patients)
CRESTOR (70 patients)
BISOPROLOL FUMARATE (70 patients)
ONDANSETRON (70 patients)
PURSENNID (69 patients)
FORTEO (69 patients)
NYSTATIN (69 patients)
TOPROL-XL (69 patients)
VALIUM (69 patients)
NEUPOGEN (68 patients)
NEORAL (68 patients)
TAVOR (68 patients)
Most common side effects for patients taking ALMARL:
DEPRESSED LEVEL OF CONSCIOUSNESS (20 patients)
HALLUCINATION (15 patients)
FALL (13 patients)
HYPOGLYCAEMIA (13 patients)
PYREXIA (12 patients)
TREMOR (12 patients)
DIARRHOEA (11 patients)
HEPATIC FUNCTION ABNORMAL (11 patients)
PNEUMONIA (10 patients)
DYSARTHRIA (10 patients)
BLOOD CREATINE PHOSPHOKINASE INCREASED (9 patients)
RENAL FAILURE ACUTE (9 patients)
LIVER DISORDER (9 patients)
CEREBRAL INFARCTION (8 patients)
DISSEMINATED INTRAVASCULAR COAGULATION (8 patients)
DRUG INEFFECTIVE (8 patients)
RENAL IMPAIRMENT (8 patients)
HYPONATRAEMIA (8 patients)
INTERSTITIAL LUNG DISEASE (8 patients)
JAUNDICE (8 patients)
OEDEMA PERIPHERAL (8 patients)
CONDITION AGGRAVATED (7 patients)
DELIRIUM (7 patients)
DYSPHAGIA (7 patients)
DYSPNOEA (7 patients)
HYPOAESTHESIA (7 patients)
RHABDOMYOLYSIS (7 patients)
VOMITING (6 patients)
DELUSION (6 patients)
RESPIRATORY FAILURE (6 patients)
DYSKINESIA (6 patients)
SOMNOLENCE (6 patients)
HEPATIC NEOPLASM MALIGNANT (6 patients)
HYPERGLYCAEMIA (6 patients)
HYPOKALAEMIA (6 patients)
MOVEMENT DISORDER (6 patients)
MUSCULAR WEAKNESS (6 patients)
WHITE BLOOD CELL COUNT INCREASED (5 patients)
BLADDER CANCER (5 patients)
BLOOD ANTIDIURETIC HORMONE INCREASED (5 patients)
RESTLESSNESS (5 patients)
BLOOD OSMOLARITY DECREASED (5 patients)
PLEURAL EFFUSION (5 patients)
C-REACTIVE PROTEIN INCREASED (5 patients)
CONVULSION (5 patients)
RENAL DISORDER (5 patients)
VITH NERVE PARALYSIS (5 patients)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION (5 patients)
INTESTINAL OBSTRUCTION (5 patients)
SEPSIS (5 patients)
ROAD TRAFFIC ACCIDENT (5 patients)
MUSCULOSKELETAL PAIN (5 patients)
NAUSEA (5 patients)
ANOREXIA (4 patients)
ATELECTASIS (4 patients)
ATRIAL FIBRILLATION (4 patients)
ATRIOVENTRICULAR BLOCK (4 patients)
BLOOD CREATININE INCREASED (4 patients)
BRADYCARDIA (4 patients)
CARDIAC FAILURE (4 patients)
CONSTIPATION (4 patients)
DECREASED APPETITE (4 patients)
DEHYDRATION (4 patients)
DIZZINESS (4 patients)
PLATELET COUNT DECREASED (4 patients)
PAIN (4 patients)
HYPERTENSION (4 patients)
HYPOTHYROIDISM (4 patients)
ILEUS (4 patients)
METABOLIC ACIDOSIS (4 patients)
SMALL INTESTINE CARCINOMA (4 patients)
URINE OSMOLARITY INCREASED (4 patients)
ABASIA (3 patients)
AGGRESSION (3 patients)
PRURITUS (3 patients)
ANAEMIA (3 patients)
PULMONARY ALVEOLAR HAEMORRHAGE (3 patients)
WHITE BLOOD CELL COUNT DECREASED (3 patients)
ASTHMA (3 patients)
BLOOD BILIRUBIN INCREASED (3 patients)
RENAL FAILURE (3 patients)
BLOOD PRESSURE DECREASED (3 patients)
BLOOD PRESSURE INCREASED (3 patients)
VASCULITIS (3 patients)
CAROTID ARTERY STENOSIS (3 patients)
THERAPEUTIC AGENT TOXICITY (3 patients)
CHILLS (3 patients)
CHROMATURIA (3 patients)
PETECHIAE (3 patients)
CHRONIC LYMPHOCYTIC LEUKAEMIA (3 patients)
PORIOMANIA (3 patients)
RENAL ARTERY STENOSIS (3 patients)
PANCYTOPENIA (3 patients)
DRUG ERUPTION (3 patients)
SUDDEN ONSET OF SLEEP (3 patients)
DRUG WITHDRAWAL SYNDROME (3 patients)
VERTIGO (3 patients)
EPILEPSY (3 patients)
FACE OEDEMA (3 patients)
VOLVULUS (3 patients)
GENERALISED OEDEMA (3 patients)
GINGIVAL BLEEDING (3 patients)
HAEMORRHAGE SUBCUTANEOUS (3 patients)
HALLUCINATION, VISUAL (3 patients)
PSYCHIATRIC SYMPTOM (3 patients)
HEART RATE DECREASED (3 patients)
HELICOBACTER TEST POSITIVE (3 patients)
HEPATITIS FULMINANT (3 patients)
HYPERKALAEMIA (3 patients)
HYPOTENSION (3 patients)
IDIOPATHIC THROMBOCYTOPENIC PURPURA (3 patients)
LOSS OF CONSCIOUSNESS (3 patients)
SENSORY DISTURBANCE (3 patients)
LYMPHOMA (3 patients)
MALAISE (3 patients)
MARKEDLY REDUCED DIETARY INTAKE (3 patients)
RENAL TUBULAR DISORDER (3 patients)
NEOPLASM MALIGNANT (3 patients)
SINUS ARREST (3 patients)
ABDOMINAL DISCOMFORT (2 patients)
ABDOMINAL PAIN (2 patients)
ACUTE MYELOID LEUKAEMIA (2 patients)
STOMACH MASS (2 patients)
PERSONALITY CHANGE (2 patients)
AGITATION (2 patients)
ALTERED STATE OF CONSCIOUSNESS (2 patients)
ANAPHYLACTOID REACTION (2 patients)
ANGER (2 patients)
PRODUCTIVE COUGH (2 patients)
RENAL CYST (2 patients)
APHASIA (2 patients)
ASTHENIA (2 patients)
ATRIOVENTRICULAR BLOCK COMPLETE (2 patients)
THIRST (2 patients)
PROSTATE CANCER (2 patients)
BLOOD AMYLASE INCREASED (2 patients)
BLOOD UREA INCREASED (2 patients)
BODY TEMPERATURE INCREASED (2 patients)
SPEECH DISORDER (2 patients)
TUMOUR LYSIS SYNDROME (2 patients)
CEREBRAL HAEMORRHAGE (2 patients)
CHEST X-RAY ABNORMAL (2 patients)
COLON CANCER (2 patients)
COMA HEPATIC (2 patients)
COMPLETED SUICIDE (2 patients)
CONTUSION (2 patients)
PERFORMANCE STATUS DECREASED (2 patients)
DEFAECATION URGENCY (2 patients)
DEMENTIA ALZHEIMER'S TYPE (2 patients)
RASH PRURITIC (2 patients)
DIABETIC KETOACIDOSIS (2 patients)
DRUG INTERACTION (2 patients)
DRUG LEVEL INCREASED (2 patients)
DYSPEPSIA (2 patients)
DYSSTASIA (2 patients)
ELECTROCARDIOGRAM QT PROLONGED (2 patients)
STEVENS-JOHNSON SYNDROME (2 patients)
EPULIS (2 patients)
EXTRAOCULAR MUSCLE PARESIS (2 patients)
FACIAL PARESIS (2 patients)
FEAR (2 patients)
FEBRILE NEUTROPENIA (2 patients)
FEMORAL NECK FRACTURE (2 patients)
FOOT FRACTURE (2 patients)
GAMMA-GLUTAMYLTRANSFERASE INCREASED (2 patients)
GANGRENE (2 patients)
GASTRIC ULCER HAEMORRHAGE (2 patients)
GINGIVAL HYPERTROPHY (2 patients)
GLOSSOPTOSIS (2 patients)
PLEURISY (2 patients)
PHRENIC NERVE PARALYSIS (2 patients)
HAEMATEMESIS (2 patients)
HAEMATURIA (2 patients)
HAEMOGLOBIN DECREASED (2 patients)
POLLAKIURIA (2 patients)
ORAL INTAKE REDUCED (2 patients)
HEPATIC CYST (2 patients)
HEPATIC ENCEPHALOPATHY (2 patients)
HEPATITIS (2 patients)
HYPERREFLEXIA (2 patients)
HYPERTONIA (2 patients)
HYPERURICAEMIA (2 patients)
RASH PAPULAR (2 patients)
INITIAL INSOMNIA (2 patients)
RETINAL OEDEMA (2 patients)
INTESTINAL FUNCTIONAL DISORDER (2 patients)
RESPIRATION ABNORMAL (2 patients)
IRRITABILITY (2 patients)
RIB FRACTURE (2 patients)
LEG AMPUTATION (2 patients)
LYMPHADENOPATHY (2 patients)
METABOLIC ALKALOSIS (2 patients)
ORAL HERPES (2 patients)
TAKAYASU'S ARTERITIS (2 patients)
MOUTH HAEMORRHAGE (2 patients)
UNRESPONSIVE TO STIMULI (2 patients)
TOXIC SKIN ERUPTION (2 patients)
NEPHROLITHIASIS (2 patients)
SUICIDE ATTEMPT (2 patients)
VENTRICULAR FIBRILLATION (2 patients)
NEUTROPHIL COUNT DECREASED (2 patients)
UPPER RESPIRATORY TRACT INFECTION (2 patients)
UPPER GASTROINTESTINAL HAEMORRHAGE (2 patients)
SHOCK HAEMORRHAGIC (2 patients)
ABDOMEN CRUSHING (1 patients)
CARDIAC FAILURE CONGESTIVE (1 patients)
EOSINOPHILIC PNEUMONIA ACUTE (1 patients)
ESSENTIAL TREMOR (1 patients)
WRONG TECHNIQUE IN DRUG USAGE PROCESS (1 patients)
FUNGAL INFECTION (1 patients)

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