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

NAUSEA ( 68 FDA reports)
ANXIETY ( 54 FDA reports)
PAIN ( 53 FDA reports)
DEEP VEIN THROMBOSIS ( 47 FDA reports)
ARTHRALGIA ( 45 FDA reports)
DEPRESSION ( 45 FDA reports)
DYSPNOEA ( 44 FDA reports)
FATIGUE ( 42 FDA reports)
HEADACHE ( 41 FDA reports)
VOMITING ( 41 FDA reports)
CHEST PAIN ( 40 FDA reports)
INSOMNIA ( 40 FDA reports)
PAIN IN EXTREMITY ( 38 FDA reports)
PULMONARY EMBOLISM ( 38 FDA reports)
NIGHT SWEATS ( 34 FDA reports)
BRONCHITIS ( 33 FDA reports)
ABDOMINAL PAIN UPPER ( 32 FDA reports)
ASTHENIA ( 29 FDA reports)
BACK PAIN ( 29 FDA reports)
DIZZINESS ( 29 FDA reports)
WEIGHT DECREASED ( 28 FDA reports)
CHOLECYSTITIS CHRONIC ( 27 FDA reports)
INJURY ( 26 FDA reports)
SINUSITIS ( 26 FDA reports)
OSTEOARTHRITIS ( 25 FDA reports)
RECTAL HAEMORRHAGE ( 25 FDA reports)
DRUG INEFFECTIVE ( 24 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
EMOTIONAL DISTRESS ( 23 FDA reports)
HYPOAESTHESIA ( 23 FDA reports)
SUICIDAL IDEATION ( 23 FDA reports)
HAEMORRHOIDS ( 22 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 21 FDA reports)
ABDOMINAL DISCOMFORT ( 20 FDA reports)
AMNESIA ( 20 FDA reports)
MYALGIA ( 20 FDA reports)
ANAEMIA ( 19 FDA reports)
MUSCLE SPASMS ( 19 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
COUGH ( 18 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 18 FDA reports)
MUSCLE TWITCHING ( 18 FDA reports)
OEDEMA PERIPHERAL ( 18 FDA reports)
CELLULITIS ( 17 FDA reports)
COLITIS ULCERATIVE ( 17 FDA reports)
CONSTIPATION ( 17 FDA reports)
CROHN'S DISEASE ( 17 FDA reports)
FALL ( 17 FDA reports)
GASTRITIS ( 17 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 17 FDA reports)
PARAESTHESIA ( 16 FDA reports)
DIARRHOEA ( 15 FDA reports)
DYSPEPSIA ( 15 FDA reports)
MALAISE ( 15 FDA reports)
MOOD SWINGS ( 15 FDA reports)
TENDONITIS ( 15 FDA reports)
HYPERTENSION ( 14 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 14 FDA reports)
PANCREATITIS ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
RASH ( 14 FDA reports)
VISION BLURRED ( 14 FDA reports)
DYSPHAGIA ( 13 FDA reports)
GALLBLADDER DISORDER ( 13 FDA reports)
MIGRAINE ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SLEEP APNOEA SYNDROME ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 13 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 12 FDA reports)
CONDITION AGGRAVATED ( 12 FDA reports)
CONVULSION ( 12 FDA reports)
DEAFNESS ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
FISTULA ( 12 FDA reports)
GASTROENTERITIS BACTERIAL ( 12 FDA reports)
HERPES ZOSTER ( 12 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 12 FDA reports)
PERICARDIAL EFFUSION ( 12 FDA reports)
PHOTOSENSITIVITY REACTION ( 12 FDA reports)
PLEURAL EFFUSION ( 12 FDA reports)
PROCTALGIA ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
VERTIGO ( 12 FDA reports)
ANGER ( 11 FDA reports)
ARTHRITIS INFECTIVE ( 11 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
CORONARY ARTERY DISEASE ( 11 FDA reports)
DRY MOUTH ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
LACRIMATION INCREASED ( 11 FDA reports)
METABOLIC ACIDOSIS ( 11 FDA reports)
MUSCULOSKELETAL PAIN ( 11 FDA reports)
NEUROPATHY PERIPHERAL ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 11 FDA reports)
SCROTAL CYST ( 11 FDA reports)
SWOLLEN TONGUE ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
VASCULITIS ( 11 FDA reports)
WOUND INFECTION ( 11 FDA reports)
ARTHRITIS ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
COGNITIVE DISORDER ( 10 FDA reports)
DEHYDRATION ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
FIBROMYALGIA ( 10 FDA reports)
GRAND MAL CONVULSION ( 10 FDA reports)
INFLUENZA LIKE ILLNESS ( 10 FDA reports)
JOINT CREPITATION ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
MYOSITIS ( 10 FDA reports)
RHINORRHOEA ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
TYPE 2 DIABETES MELLITUS ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 9 FDA reports)
AUTOIMMUNE DISORDER ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CONNECTIVE TISSUE DISORDER ( 9 FDA reports)
CORONARY ARTERY STENOSIS ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
DYSSTASIA ( 9 FDA reports)
EAR PAIN ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
MENTAL IMPAIRMENT ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
PHARYNGITIS ( 9 FDA reports)
PRURITUS ANI ( 9 FDA reports)
ALOPECIA ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CONJUNCTIVITIS VIRAL ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
GROIN PAIN ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
HYPERKERATOSIS ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
IRRITABLE BOWEL SYNDROME ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LUNG NEOPLASM ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
NERVE INJURY ( 8 FDA reports)
OTORRHOEA ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PLEURITIC PAIN ( 8 FDA reports)
RAYNAUD'S PHENOMENON ( 8 FDA reports)
SCIATICA ( 8 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 8 FDA reports)
TENDON RUPTURE ( 8 FDA reports)
THIRST ( 8 FDA reports)
TREMOR ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 7 FDA reports)
ACNE ( 7 FDA reports)
APHASIA ( 7 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 7 FDA reports)
ASCITES ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CEREBROVASCULAR ACCIDENT ( 7 FDA reports)
CERVICAL POLYP ( 7 FDA reports)
CERVICOBRACHIAL SYNDROME ( 7 FDA reports)
COLON ADENOMA ( 7 FDA reports)
COSTOCHONDRITIS ( 7 FDA reports)
CYST ( 7 FDA reports)
DIVERTICULUM ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
GASTRIC CANCER RECURRENT ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
HAEMATOCHEZIA ( 7 FDA reports)
HYDROCELE ( 7 FDA reports)
HYPOKALAEMIA ( 7 FDA reports)
INGUINAL HERNIA ( 7 FDA reports)
JOINT SWELLING ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
METRORRHAGIA ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MUSCLE INJURY ( 7 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 7 FDA reports)
NEUROPATHY ( 7 FDA reports)
OBSTRUCTION GASTRIC ( 7 FDA reports)
OEDEMA ( 7 FDA reports)
OESOPHAGITIS ULCERATIVE ( 7 FDA reports)
OSTEONECROSIS OF JAW ( 7 FDA reports)
PILONIDAL CYST ( 7 FDA reports)
POLYNEUROPATHY ( 7 FDA reports)
PRIMARY MEDIASTINAL LARGE B-CELL LYMPHOMA STAGE II ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
SKIN IRRITATION ( 7 FDA reports)
SPLENOMEGALY ( 7 FDA reports)
STRESS ULCER ( 7 FDA reports)
TENSION HEADACHE ( 7 FDA reports)
VIRAL LOAD INCREASED ( 7 FDA reports)
VIRAL PHARYNGITIS ( 7 FDA reports)
VISUAL DISTURBANCE ( 7 FDA reports)
ABSCESS ( 6 FDA reports)
ACCIDENT ( 6 FDA reports)
ANAL FISSURE ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
ASTHMA ( 6 FDA reports)
BIOPSY BONE MARROW ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CHRONIC FATIGUE SYNDROME ( 6 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
FALLOT'S TETRALOGY ( 6 FDA reports)
FEAR ( 6 FDA reports)
FOOD POISONING ( 6 FDA reports)
GINGIVAL PAIN ( 6 FDA reports)
GUILLAIN-BARRE SYNDROME ( 6 FDA reports)
HAEMANGIOMA OF LIVER ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
HYDROPS FOETALIS ( 6 FDA reports)
INTRA-UTERINE DEATH ( 6 FDA reports)
KELOID SCAR ( 6 FDA reports)
LOCALISED OEDEMA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MEDIASTINAL BIOPSY ( 6 FDA reports)
MEDIASTINAL MASS ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MUSCLE STRAIN ( 6 FDA reports)
MUSCULOSKELETAL DISORDER ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
ONYCHOMYCOSIS ( 6 FDA reports)
PENIS DISORDER ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
SCHIZOPHRENIA ( 6 FDA reports)
SINUS CONGESTION ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
SKIN FISSURES ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
STRESS URINARY INCONTINENCE ( 6 FDA reports)
SWELLING ( 6 FDA reports)
TENDON DISORDER ( 6 FDA reports)
THROMBOSIS ( 6 FDA reports)
TONGUE DRY ( 6 FDA reports)
VARICOSE VEIN ( 6 FDA reports)
VENTRICULAR HYPERTROPHY ( 6 FDA reports)
XEROSIS ( 6 FDA reports)
ACOUSTIC STIMULATION TESTS ABNORMAL ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
ANHEDONIA ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 5 FDA reports)
BRACHIAL PLEXUS INJURY ( 5 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 5 FDA reports)
CATHETER PLACEMENT ( 5 FDA reports)
CHOLESTEROSIS ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
ECZEMA ASTEATOTIC ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
GASTRECTOMY ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HERPES SIMPLEX ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
IRITIS ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
JOINT DISLOCATION ( 5 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
MEMORY IMPAIRMENT ( 5 FDA reports)
MENINGITIS ( 5 FDA reports)
MITRAL VALVE PROLAPSE ( 5 FDA reports)
MOBILITY DECREASED ( 5 FDA reports)
MOTOR DYSFUNCTION ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
NO ADVERSE EFFECT ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
POOR QUALITY SLEEP ( 5 FDA reports)
POST HERPETIC NEURALGIA ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SEQUESTRECTOMY ( 5 FDA reports)
SPINAL DECOMPRESSION ( 5 FDA reports)
SPINAL LAMINECTOMY ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
THROAT TIGHTNESS ( 5 FDA reports)
TINEA PEDIS ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
VAGOTOMY ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
DEATH ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DISABILITY ( 4 FDA reports)
DYSPNOEA EXERTIONAL ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HELICOBACTER TEST POSITIVE ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INGROWING NAIL ( 4 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 4 FDA reports)
LYMPHOMA ( 4 FDA reports)
MACULOPATHY ( 4 FDA reports)
MOTION SICKNESS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYOCARDITIS ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PROTEIN TOTAL INCREASED ( 4 FDA reports)
PULMONARY CALCIFICATION ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 4 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
RHEUMATOID FACTOR INCREASED ( 4 FDA reports)
ROTATOR CUFF SYNDROME ( 4 FDA reports)
SCAR ( 4 FDA reports)
SCOLIOSIS ( 4 FDA reports)
SEBORRHOEIC DERMATITIS ( 4 FDA reports)
SEMINAL VESICULITIS ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SINUS DISORDER ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SKIN LACERATION ( 4 FDA reports)
SKIN OEDEMA ( 4 FDA reports)
SKIN PAPILLOMA ( 4 FDA reports)
SPLENIC INFARCTION ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 4 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
THYROID DISORDER ( 4 FDA reports)
TINEA CAPITIS ( 4 FDA reports)
VAGINAL DISCHARGE ( 4 FDA reports)
ANAL DISCOMFORT ( 3 FDA reports)
ANAL FUNGAL INFECTION ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
APPLICATION SITE IRRITATION ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE PAIN ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BURSA DISORDER ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CHLAMYDIAL INFECTION ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
DECREASED INTEREST ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DEPENDENCE ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSGRAPHIA ( 3 FDA reports)
ENCEPHALOMALACIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FURUNCLE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYDRONEPHROSIS ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERLIPIDAEMIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFECTED VARICOSE VEIN ( 3 FDA reports)
IUCD COMPLICATION ( 3 FDA reports)
IUD MIGRATION ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MAJOR DEPRESSION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
METASTASES TO BONE ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
NASAL SINUS DRAINAGE ( 3 FDA reports)
NERVE ROOT COMPRESSION ( 3 FDA reports)
NEUROPSYCHOLOGICAL TEST ABNORMAL ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
ORGAN FAILURE ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OTITIS MEDIA ACUTE ( 3 FDA reports)
PANCREATIC CARCINOMA ( 3 FDA reports)
PANCREATIC PSEUDOCYST ( 3 FDA reports)
PANCREATITIS NECROTISING ( 3 FDA reports)
PARALYSIS ( 3 FDA reports)
PELVIC VENOUS THROMBOSIS ( 3 FDA reports)
POSTNASAL DRIP ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PROCTITIS HERPES ( 3 FDA reports)
PSEUDOPOLYPOSIS ( 3 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
RHABDOMYOLYSIS ( 3 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 3 FDA reports)
RHINITIS ALLERGIC ( 3 FDA reports)
SELF-MEDICATION ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBCUTANEOUS ABSCESS ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
THERMAL BURN ( 3 FDA reports)
THROMBOCYTOSIS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ACANTHOMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAL FISTULA ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BREAST CANCER IN SITU ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CERVICAL CYST ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEMYELINATION ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
EPICONDYLITIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
FACET JOINT SYNDROME ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GRIP STRENGTH DECREASED ( 2 FDA reports)
GUN SHOT WOUND ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMATOSPERMIA ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL SELF-INJURY ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
MITRAL VALVE STENOSIS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 2 FDA reports)
OVARIAN CYST RUPTURED ( 2 FDA reports)
PANCREATIC PHLEGMON ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PILOERECTION ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOPOLYP ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
PUNCTATE KERATITIS ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RETINAL TOXICITY ( 2 FDA reports)
RETINOPATHY ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
SYNOVIAL FLUID ANALYSIS ABNORMAL ( 2 FDA reports)
SYNOVITIS ( 2 FDA reports)
TESTICULAR DISORDER ( 2 FDA reports)
THROMBOCYTHAEMIA ( 2 FDA reports)
TRICUSPID VALVE STENOSIS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABSCESS INTESTINAL ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ADENOMYOSIS ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGNOSIA ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ARTHROPOD BITE ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIAL SECRETION RETENTION ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMOSIDERIN DEPOSITION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONGENITAL PULMONARY VALVE DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CSF TEST ABNORMAL ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DACRYOCYSTITIS INFECTIVE ( 1 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA STAGE II ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DRUG ADDICT ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
ELECTRIC SHOCK ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACIAL WASTING ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
GASTRIC OUTLET OBSTRUCTION ( 1 FDA reports)
GASTRIC PH DECREASED ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSURIA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS C VIRUS ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEAL FISTULA ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INGROWN HAIR ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACRANIAL ANEURYSM ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB DEFORMITY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
MASS ( 1 FDA reports)
MENOMETRORRHAGIA ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY ( 1 FDA reports)
MIDDLE EAR DISORDER ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATELLA REPLACEMENT ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PECTUS EXCAVATUM ( 1 FDA reports)
PENIS DEVIATION ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMATURIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SCROTAL DISORDER ( 1 FDA reports)
SEMINAL VESICULAR DISORDER ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPERMATORRHOEA ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL X-RAY ABNORMAL ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY FISTULA ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICOCELE REPAIR ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VESICAL FISTULA ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WALKING DISTANCE TEST ABNORMAL ( 1 FDA reports)
WEIGHT BEARING DIFFICULTY ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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