Please choose an event type to view the corresponding MedsFacts report:

DEPRESSION ( 52 FDA reports)
DRUG INEFFECTIVE ( 43 FDA reports)
WEIGHT INCREASED ( 32 FDA reports)
FATIGUE ( 30 FDA reports)
NAUSEA ( 30 FDA reports)
INSOMNIA ( 28 FDA reports)
WEIGHT DECREASED ( 28 FDA reports)
VOMITING ( 27 FDA reports)
SOMNOLENCE ( 26 FDA reports)
ANXIETY ( 25 FDA reports)
DIZZINESS ( 24 FDA reports)
HEADACHE ( 22 FDA reports)
MALAISE ( 21 FDA reports)
TREMOR ( 20 FDA reports)
DYSPNOEA ( 19 FDA reports)
OVERDOSE ( 19 FDA reports)
SUICIDAL IDEATION ( 19 FDA reports)
ASTHENIA ( 18 FDA reports)
CEREBROVASCULAR ACCIDENT ( 18 FDA reports)
CONVULSION ( 18 FDA reports)
TARDIVE DYSKINESIA ( 18 FDA reports)
DIARRHOEA ( 17 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 16 FDA reports)
FALL ( 15 FDA reports)
HYPOTENSION ( 14 FDA reports)
OFF LABEL USE ( 14 FDA reports)
PAIN ( 14 FDA reports)
PYREXIA ( 14 FDA reports)
SUICIDE ATTEMPT ( 14 FDA reports)
BACK PAIN ( 13 FDA reports)
DEHYDRATION ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
RASH ( 13 FDA reports)
COMPLETED SUICIDE ( 12 FDA reports)
INTENTIONAL DRUG MISUSE ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
AGGRESSION ( 11 FDA reports)
AMNESIA ( 11 FDA reports)
ANAEMIA ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
HOT FLUSH ( 11 FDA reports)
CONSTIPATION ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
DEATH ( 10 FDA reports)
DRUG TOXICITY ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
CHILLS ( 9 FDA reports)
DRUG DOSE OMISSION ( 9 FDA reports)
MANIA ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
DRUG DEPENDENCE ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
FAECES DISCOLOURED ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
AKATHISIA ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CONGENITAL TRICUSPID VALVE STENOSIS ( 7 FDA reports)
DEPRESSED MOOD ( 7 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOPLASTIC RIGHT HEART SYNDROME ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
NIGHT SWEATS ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
ROAD TRAFFIC ACCIDENT ( 7 FDA reports)
STRESS ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABASIA ( 6 FDA reports)
AGITATION ( 6 FDA reports)
ANGER ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
DYSPEPSIA ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
INCORRECT DOSE ADMINISTERED ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
SEPSIS ( 6 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLADDER CANCER ( 5 FDA reports)
COLON CANCER ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HOMICIDAL IDEATION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NERVOUSNESS ( 5 FDA reports)
OPTIC NEURITIS ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PSYCHOTIC DISORDER ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SEDATION ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
SLEEP DISORDER ( 5 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ALOPECIA ( 4 FDA reports)
APATHY ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
FACIAL BONES FRACTURE ( 4 FDA reports)
FEAR ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
IMPAIRED HEALING ( 4 FDA reports)
IMPAIRED SELF-CARE ( 4 FDA reports)
INFLUENZA ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
MASTOCYTOSIS ( 4 FDA reports)
MEDICAL DEVICE PAIN ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OPTIC NEUROPATHY ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SPINAL OSTEOARTHRITIS ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
CRYING ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETIC COMA ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HALLUCINATION, AUDITORY ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOVITAMINOSIS ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MASS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
METASTATIC NEOPLASM ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PAPILLOEDEMA ( 3 FDA reports)
PERFORATED ULCER ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
REBOUND EFFECT ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SOMNAMBULISM ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
SPONDYLOLISTHESIS ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TENSION ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
BLADDER DISORDER ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST CALCIFICATIONS ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONCUSSION ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYST ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPAREUNIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EXCESSIVE EYE BLINKING ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FEBRILE INFECTION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATITIS C ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOMANIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE NODULE ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NO ADVERSE EVENT ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OBESITY SURGERY ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
PREGNANCY TEST URINE POSITIVE ( 2 FDA reports)
PRODUCT ADHESION ISSUE ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY MYCOSIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL COLIC ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SCLERAL PIGMENTATION ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TEMPORAL ARTERITIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTH LOSS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VAGINAL DISORDER ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PAPULES ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
BACTERIAL PYELONEPHRITIS ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BREAST HAEMORRHAGE ( 1 FDA reports)
BREAST HYPERPLASIA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC OPERATION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL ULCER ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
DEFAECATION URGENCY ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERTIONAL HEADACHE ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL ASYMMETRY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAMILIAL TREMOR ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
H1N1 INFLUENZA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILLITERACY ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOB DISSATISFACTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT LOCK ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOCYTE COUNT NORMAL ( 1 FDA reports)
MACULE ( 1 FDA reports)
MAGICAL THINKING ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICAL INDUCTION OF COMA ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUTISM ( 1 FDA reports)
NEPHROCALCINOSIS ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTINFARCTION ANGINA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA VERSICOLOUR ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR EMBOLISM ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL NEOPLASM ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHIPLASH INJURY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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