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

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, 3 individuals taking ALMARL reported CHILLS 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 CHILLS. In doing so, we compare ALMARL with other drugs that cause CHILLS, to help you evaluate whether or not ALMARL causes CHILLS. Likewise, this page shows the most highly-reported side effects of ALMARL, so you can see if CHILLS ranks among ALMARL's most well-known side effects.
Summary Statistics
Reports of ALMARL causing CHILLS: 3
Reports of any side effect of ALMARL : 227
Percentage of ALMARL patients where CHILLS is a reported side effect: 1.3216%

FDA reports of any drug causing CHILLS : 33540
Average percentage for all medicated patients where CHILLS is reported as a complication: 0.2102%

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 CHILLS:

ASPIRIN (2154 patients)
REMICADE (2099 patients)
HEPARIN SODIUM INJECTION (1818 patients)
HUMIRA (1793 patients)
AVONEX (1709 patients)
PREDNISONE (1327 patients)
ENBREL (1245 patients)
METHOTREXATE (1047 patients)
NEXIUM (980 patients)
ZOMETA (975 patients)
ACETAMINOPHEN (964 patients)
SYNTHROID (928 patients)
LIPITOR (895 patients)
FOSAMAX (878 patients)
FOLIC ACID (872 patients)
TYSABRI (864 patients)
LISINOPRIL (806 patients)
OMEPRAZOLE (796 patients)
REBIF (772 patients)
LASIX (772 patients)
OXYCONTIN (748 patients)
VITAMIN D (722 patients)
PRILOSEC (715 patients)
ATENOLOL (702 patients)
SANDOSTATIN LAR (701 patients)
BENADRYL (688 patients)
BYETTA (664 patients)
GAMMAGARD LIQUID (657 patients)
BETASERON (653 patients)
PREDNISOLONE (647 patients)
NEURONTIN (646 patients)
AMBIEN (642 patients)
XANAX (640 patients)
SIMVASTATIN (637 patients)
PEGASYS (633 patients)
IBUPROFEN (626 patients)
PAXIL (606 patients)
ZOFRAN (600 patients)
COUMADIN (588 patients)
CYMBALTA (587 patients)
HYDROCHLOROTHIAZIDE (580 patients)
NORVASC (580 patients)
SEROQUEL (575 patients)
PROTONIX (573 patients)
PLAVIX (565 patients)
PREDNISONE TAB (562 patients)
ATIVAN (555 patients)
ALBUTEROL (553 patients)
DEXAMETHASONE (553 patients)
LEVOTHYROXINE SODIUM (548 patients)
LYRICA (547 patients)
RIBAVIRIN (544 patients)
POTASSIUM CHLORIDE (529 patients)
ALLOPURINOL (526 patients)
FUROSEMIDE (514 patients)
DURAGESIC-100 (512 patients)
VIOXX (511 patients)
CALCIUM (499 patients)
RECLAST (498 patients)
LEVAQUIN (491 patients)
ZOLOFT (489 patients)
LORAZEPAM (488 patients)
FORTEO (486 patients)
VICODIN (481 patients)
CYCLOPHOSPHAMIDE (472 patients)
METFORMIN HCL (471 patients)
CELEBREX (459 patients)
GABAPENTIN (451 patients)
PERCOCET (449 patients)
PREVACID (439 patients)
ZOCOR (430 patients)
LEXAPRO (429 patients)
TOPROL-XL (427 patients)
DECADRON (419 patients)
TYLENOL (409 patients)
FLUOROURACIL (407 patients)
CRESTOR (405 patients)
CARBOPLATIN (404 patients)
HEPARIN SODIUM (400 patients)
CLONAZEPAM (400 patients)
OXYCODONE HCL (399 patients)
MULTI-VITAMINS (397 patients)
EXTAVIA (392 patients)
METOPROLOL TARTRATE (392 patients)
FABRAZYME (391 patients)
ACCUTANE (379 patients)
MORPHINE (378 patients)
DIOVAN (365 patients)
VANCOMYCIN (365 patients)
AREDIA (363 patients)
SOLIRIS (359 patients)
PREMARIN (357 patients)
DIGOXIN (357 patients)
TYLENOL (CAPLET) (352 patients)
CHANTIX (351 patients)
SINGULAIR (350 patients)
ADVAIR DISKUS 100/50 (345 patients)
EFFEXOR (344 patients)
EXJADE (340 patients)
KLONOPIN (335 patients)
LANTUS (334 patients)
NIASPAN (334 patients)
PEG-INTRON (328 patients)
ACYCLOVIR (324 patients)
FENTANYL (323 patients)
MULTI-VITAMIN (322 patients)
PROZAC (321 patients)
CELEXA (319 patients)
AMLODIPINE (319 patients)
CISPLATIN (318 patients)
BACTRIM (315 patients)
REVLIMID (311 patients)
VALIUM (305 patients)
COMPAZINE (300 patients)
DIAZEPAM (298 patients)
ZYRTEC (294 patients)
VELCADE (294 patients)
ZANTAC (292 patients)
ACTONEL (289 patients)
ZITHROMAX (286 patients)
TRAMADOL HCL (285 patients)
COPEGUS (285 patients)
INSULIN (284 patients)
LORTAB (278 patients)
WARFARIN SODIUM (277 patients)
ALLEGRA (274 patients)
AVASTIN (273 patients)
FLUCONAZOLE (272 patients)
PROPOFOL (272 patients)
BONIVA (272 patients)
RITUXIMAB (271 patients)
PANTOPRAZOLE (265 patients)
LAMICTAL (260 patients)
TRAZODONE HCL (260 patients)
ACLASTA (259 patients)
TAXOTERE (258 patients)
CIPROFLOXACIN (258 patients)
RADIATION THERAPY (257 patients)
WELLBUTRIN (256 patients)
TAXOL (256 patients)
CALCIUM CARBONATE (256 patients)
FLEXERIL (255 patients)
ALPRAZOLAM (253 patients)
FISH OIL (250 patients)
EFFEXOR XR (248 patients)
ARANESP (247 patients)
AUGMENTIN '125' (246 patients)
NITROGLYCERIN (246 patients)
ASCORBIC ACID (245 patients)
FLOMAX (244 patients)
BACLOFEN (243 patients)
COREG (243 patients)
GLUCOPHAGE (242 patients)
MYLOTARG (242 patients)
RITUXAN (242 patients)
SPIRIVA (240 patients)
AVELOX (240 patients)
METOPROLOL (237 patients)
THYMOGLOBULIN (236 patients)
DOXORUBICIN HCL (232 patients)
FLAGYL (229 patients)
ERBITUX (228 patients)
SOLU-MEDROL (227 patients)
COZAAR (227 patients)
AMOXICILLIN (226 patients)
INCIVEK (224 patients)
DILAUDID (222 patients)
PEPCID (219 patients)
GLIPIZIDE (218 patients)
REGLAN (217 patients)
IRON (216 patients)
GLYBURIDE (215 patients)
OXALIPLATIN (214 patients)
NEUPOGEN (214 patients)
METFORMIN (212 patients)
LANSOPRAZOLE (211 patients)
RANITIDINE (211 patients)
AMITRIPTYLINE HCL (210 patients)
VITAMIN B-12 (209 patients)
VOLTAREN (209 patients)
ZOLEDRONOC ACID (207 patients)
COLACE (205 patients)
LOVENOX (204 patients)
ENALAPRIL MALEATE (203 patients)
CLONIDINE (202 patients)
CYTARABINE (200 patients)
CYCLOSPORINE (200 patients)
ACTOS (200 patients)
MORPHINE SULFATE (197 patients)
HYDROCORTISONE (197 patients)
DIFLUCAN (197 patients)
RAMIPRIL (196 patients)
NAPROXEN (196 patients)
CIPRO (196 patients)
GILENYA (195 patients)
PROCRIT (194 patients)
MIRALAX (194 patients)
VINCRISTINE (193 patients)
FLONASE (192 patients)
HERCEPTIN (192 patients)
LEVOXYL (192 patients)
HEPARIN (189 patients)
LEUCOVORIN CALCIUM (189 patients)
PACLITAXEL (187 patients)
PLAQUENIL (186 patients)
MOBIC (184 patients)
GLEEVEC (184 patients)
ETOPOSIDE (183 patients)
MS CONTIN (183 patients)
MABTHERA (182 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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