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

CONVULSION ( 445 FDA reports)
FALL ( 408 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 361 FDA reports)
GAIT DISTURBANCE ( 359 FDA reports)
FATIGUE ( 331 FDA reports)
URINARY TRACT INFECTION ( 300 FDA reports)
BALANCE DISORDER ( 277 FDA reports)
DIZZINESS ( 256 FDA reports)
ASTHENIA ( 248 FDA reports)
NAUSEA ( 212 FDA reports)
HEADACHE ( 206 FDA reports)
MUSCULAR WEAKNESS ( 186 FDA reports)
ABASIA ( 183 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 175 FDA reports)
INSOMNIA ( 166 FDA reports)
DRUG INEFFECTIVE ( 145 FDA reports)
TREMOR ( 144 FDA reports)
DEPRESSION ( 137 FDA reports)
FEELING ABNORMAL ( 125 FDA reports)
CONDITION AGGRAVATED ( 124 FDA reports)
BACK PAIN ( 123 FDA reports)
LOSS OF CONSCIOUSNESS ( 123 FDA reports)
MULTIPLE SCLEROSIS ( 123 FDA reports)
HYPOAESTHESIA ( 119 FDA reports)
MUSCLE SPASMS ( 117 FDA reports)
PAIN IN EXTREMITY ( 115 FDA reports)
CONFUSIONAL STATE ( 109 FDA reports)
PAIN ( 109 FDA reports)
PARAESTHESIA ( 101 FDA reports)
DYSPNOEA ( 94 FDA reports)
MOBILITY DECREASED ( 90 FDA reports)
OEDEMA PERIPHERAL ( 89 FDA reports)
CONSTIPATION ( 86 FDA reports)
MEMORY IMPAIRMENT ( 84 FDA reports)
INFLUENZA LIKE ILLNESS ( 83 FDA reports)
DYSSTASIA ( 77 FDA reports)
VOMITING ( 75 FDA reports)
ARTHRALGIA ( 72 FDA reports)
NEPHROLITHIASIS ( 67 FDA reports)
URINARY INCONTINENCE ( 63 FDA reports)
GRAND MAL CONVULSION ( 62 FDA reports)
MALAISE ( 62 FDA reports)
PYREXIA ( 62 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 60 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 60 FDA reports)
SYNCOPE ( 60 FDA reports)
CONTUSION ( 59 FDA reports)
PNEUMONIA ( 57 FDA reports)
DIARRHOEA ( 56 FDA reports)
CYSTITIS ( 54 FDA reports)
VISION BLURRED ( 54 FDA reports)
AMNESIA ( 53 FDA reports)
INJECTION SITE ERYTHEMA ( 53 FDA reports)
DISORIENTATION ( 51 FDA reports)
ABDOMINAL DISCOMFORT ( 50 FDA reports)
COORDINATION ABNORMAL ( 49 FDA reports)
DRUG EFFECT DECREASED ( 49 FDA reports)
HEAD INJURY ( 49 FDA reports)
SPEECH DISORDER ( 49 FDA reports)
WEIGHT DECREASED ( 48 FDA reports)
ANXIETY ( 47 FDA reports)
BURNING SENSATION ( 46 FDA reports)
INJECTION SITE HAEMATOMA ( 46 FDA reports)
NASOPHARYNGITIS ( 45 FDA reports)
VISUAL IMPAIRMENT ( 44 FDA reports)
DEATH ( 43 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 42 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 41 FDA reports)
PRURITUS ( 40 FDA reports)
STRESS ( 40 FDA reports)
HYPERTENSION ( 39 FDA reports)
HYPERHIDROSIS ( 37 FDA reports)
CHEST PAIN ( 35 FDA reports)
HALLUCINATION ( 35 FDA reports)
HEMIPARESIS ( 35 FDA reports)
INJECTION SITE PAIN ( 35 FDA reports)
VERTIGO ( 35 FDA reports)
DECREASED APPETITE ( 34 FDA reports)
COGNITIVE DISORDER ( 33 FDA reports)
ABDOMINAL PAIN ( 32 FDA reports)
MUSCLE SPASTICITY ( 32 FDA reports)
OROPHARYNGEAL PAIN ( 32 FDA reports)
UNRESPONSIVE TO STIMULI ( 32 FDA reports)
BREAST CANCER ( 31 FDA reports)
COUGH ( 31 FDA reports)
JOINT SWELLING ( 31 FDA reports)
APHASIA ( 30 FDA reports)
SUICIDAL IDEATION ( 30 FDA reports)
URTICARIA ( 30 FDA reports)
CHILLS ( 29 FDA reports)
DRUG DOSE OMISSION ( 29 FDA reports)
FEELING COLD ( 29 FDA reports)
MYALGIA ( 28 FDA reports)
NODULE ( 28 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BREAST ABNORMAL ( 28 FDA reports)
SINUSITIS ( 28 FDA reports)
CHEST DISCOMFORT ( 26 FDA reports)
HYPERSENSITIVITY ( 26 FDA reports)
HYPOTENSION ( 26 FDA reports)
MENTAL STATUS CHANGES ( 26 FDA reports)
ALOPECIA ( 25 FDA reports)
DRUG HYPERSENSITIVITY ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
HYPERVENTILATION ( 25 FDA reports)
ROAD TRAFFIC ACCIDENT ( 25 FDA reports)
ERYTHEMA ( 24 FDA reports)
FEELING HOT ( 24 FDA reports)
KIDNEY INFECTION ( 24 FDA reports)
PERIPHERAL COLDNESS ( 24 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 24 FDA reports)
ACCIDENTAL OVERDOSE ( 23 FDA reports)
EATING DISORDER ( 23 FDA reports)
RENAL FAILURE ACUTE ( 23 FDA reports)
TONGUE BITING ( 23 FDA reports)
FOOT FRACTURE ( 22 FDA reports)
MOVEMENT DISORDER ( 22 FDA reports)
POLLAKIURIA ( 22 FDA reports)
POOR VENOUS ACCESS ( 22 FDA reports)
SEPSIS ( 22 FDA reports)
THROMBOSIS ( 22 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 22 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
FLUSHING ( 21 FDA reports)
INJECTION SITE OEDEMA ( 21 FDA reports)
LOSS OF CONTROL OF LEGS ( 21 FDA reports)
PALPITATIONS ( 21 FDA reports)
RENAL DISORDER ( 21 FDA reports)
ABDOMINAL DISTENSION ( 20 FDA reports)
CRYING ( 20 FDA reports)
EYE MOVEMENT DISORDER ( 20 FDA reports)
HERPES ZOSTER ( 20 FDA reports)
MUSCULOSKELETAL DISORDER ( 20 FDA reports)
NO THERAPEUTIC RESPONSE ( 20 FDA reports)
PULMONARY EMBOLISM ( 20 FDA reports)
SENSATION OF HEAVINESS ( 20 FDA reports)
URINARY RETENTION ( 20 FDA reports)
COLITIS ( 19 FDA reports)
DISTURBANCE IN ATTENTION ( 19 FDA reports)
HIP FRACTURE ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
RASH ( 19 FDA reports)
SOMNOLENCE ( 19 FDA reports)
ADVERSE DRUG REACTION ( 18 FDA reports)
BLOOD PRESSURE INCREASED ( 18 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
NECK PAIN ( 18 FDA reports)
SENSORY DISTURBANCE ( 18 FDA reports)
WEIGHT INCREASED ( 18 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
DRY MOUTH ( 17 FDA reports)
DYSPEPSIA ( 17 FDA reports)
MENTAL IMPAIRMENT ( 17 FDA reports)
AGITATION ( 16 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 16 FDA reports)
ANGER ( 16 FDA reports)
BEDRIDDEN ( 16 FDA reports)
BLADDER DISORDER ( 16 FDA reports)
CEREBROVASCULAR ACCIDENT ( 16 FDA reports)
DYSARTHRIA ( 16 FDA reports)
DYSURIA ( 16 FDA reports)
HEPATIC ENZYME INCREASED ( 16 FDA reports)
INFLUENZA ( 16 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 16 FDA reports)
IRRITABILITY ( 16 FDA reports)
PSYCHOTIC DISORDER ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
DEPRESSED MOOD ( 15 FDA reports)
DYSKINESIA ( 15 FDA reports)
LACERATION ( 15 FDA reports)
PNEUMONIA ASPIRATION ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
AGGRESSION ( 14 FDA reports)
ANKLE FRACTURE ( 14 FDA reports)
CELLULITIS ( 14 FDA reports)
EYE PAIN ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
INCOHERENT ( 14 FDA reports)
INCORRECT DOSE ADMINISTERED ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
PERONEAL NERVE PALSY ( 14 FDA reports)
SKIN DISCOLOURATION ( 14 FDA reports)
STATUS EPILEPTICUS ( 14 FDA reports)
TEMPERATURE INTOLERANCE ( 14 FDA reports)
ANAEMIA ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
BRONCHITIS ( 13 FDA reports)
CARDIAC ARREST ( 13 FDA reports)
CATARACT ( 13 FDA reports)
DIVERTICULUM ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
FLANK PAIN ( 13 FDA reports)
HALLUCINATION, VISUAL ( 13 FDA reports)
HEART RATE DECREASED ( 13 FDA reports)
HYPOKINESIA ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
MOTOR DYSFUNCTION ( 13 FDA reports)
MUSCLE TWITCHING ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
BREAST CANCER IN SITU ( 12 FDA reports)
CAMPYLOBACTER INFECTION ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
DIPLEGIA ( 12 FDA reports)
DISEASE PROGRESSION ( 12 FDA reports)
DYSPHONIA ( 12 FDA reports)
INFECTION ( 12 FDA reports)
MENTAL DISORDER ( 12 FDA reports)
PRESYNCOPE ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
STAPHYLOCOCCAL INFECTION ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
VITAMIN D DECREASED ( 12 FDA reports)
ABNORMAL BEHAVIOUR ( 11 FDA reports)
ARTHROPATHY ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 11 FDA reports)
CHOLELITHIASIS ( 11 FDA reports)
COMA ( 11 FDA reports)
FUNGAL INFECTION ( 11 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 11 FDA reports)
HYPOAESTHESIA FACIAL ( 11 FDA reports)
INAPPROPRIATE AFFECT ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
MONOPLEGIA ( 11 FDA reports)
MUSCLE TIGHTNESS ( 11 FDA reports)
NERVOUSNESS ( 11 FDA reports)
PAIN IN JAW ( 11 FDA reports)
PERSONALITY CHANGE ( 11 FDA reports)
RENAL PAIN ( 11 FDA reports)
SLEEP DISORDER ( 11 FDA reports)
THINKING ABNORMAL ( 11 FDA reports)
THROAT IRRITATION ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
ATRIAL FIBRILLATION ( 10 FDA reports)
BLINDNESS UNILATERAL ( 10 FDA reports)
BLOOD URINE PRESENT ( 10 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 10 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 10 FDA reports)
DIPLOPIA ( 10 FDA reports)
FAECAL INCONTINENCE ( 10 FDA reports)
FEMUR FRACTURE ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HALLUCINATION, AUDITORY ( 10 FDA reports)
HYPERSOMNIA ( 10 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 10 FDA reports)
MIGRAINE ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
OFF LABEL USE ( 10 FDA reports)
PANCREATITIS ( 10 FDA reports)
PARALYSIS ( 10 FDA reports)
PRODUCT QUALITY ISSUE ( 10 FDA reports)
SKIN BURNING SENSATION ( 10 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 10 FDA reports)
SUICIDAL BEHAVIOUR ( 10 FDA reports)
UPPER LIMB FRACTURE ( 10 FDA reports)
URINE ODOUR ABNORMAL ( 10 FDA reports)
EYE DISORDER ( 9 FDA reports)
GENERAL SYMPTOM ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HAEMOGLOBIN DECREASED ( 9 FDA reports)
HEART RATE IRREGULAR ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
JOINT DISLOCATION ( 9 FDA reports)
JOINT STIFFNESS ( 9 FDA reports)
LIMB INJURY ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NIGHT SWEATS ( 9 FDA reports)
OPTIC NEURITIS ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
ROTATOR CUFF SYNDROME ( 9 FDA reports)
STARING ( 9 FDA reports)
TOOTH FRACTURE ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
BLADDER DYSFUNCTION ( 8 FDA reports)
BLINDNESS ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
BLOOD SODIUM DECREASED ( 8 FDA reports)
BODY TEMPERATURE INCREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CHOKING ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
GASTROENTERITIS VIRAL ( 8 FDA reports)
HEMIPLEGIA ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HOT FLUSH ( 8 FDA reports)
INFUSION SITE SCAR ( 8 FDA reports)
LIP INJURY ( 8 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 8 FDA reports)
LOWER LIMB FRACTURE ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
PANIC ATTACK ( 8 FDA reports)
POOR QUALITY SLEEP ( 8 FDA reports)
RASH PRURITIC ( 8 FDA reports)
RESTLESS LEGS SYNDROME ( 8 FDA reports)
SWELLING ( 8 FDA reports)
TUNNEL VISION ( 8 FDA reports)
UROSEPSIS ( 8 FDA reports)
VEIN DISORDER ( 8 FDA reports)
WALKING AID USER ( 8 FDA reports)
ABNORMAL DREAMS ( 7 FDA reports)
ADNEXA UTERI PAIN ( 7 FDA reports)
BLADDER SPASM ( 7 FDA reports)
BLEPHAROSPASM ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BLOOD MAGNESIUM DECREASED ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
BREAST CANCER FEMALE ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
CONCUSSION ( 7 FDA reports)
CONVERSION DISORDER ( 7 FDA reports)
DEMENTIA ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 7 FDA reports)
GALLBLADDER DISORDER ( 7 FDA reports)
GRIMACING ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HYPOGLYCAEMIA ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 7 FDA reports)
JOINT INJURY ( 7 FDA reports)
NASAL DISCOMFORT ( 7 FDA reports)
OSTEOARTHRITIS ( 7 FDA reports)
PHARYNGEAL OEDEMA ( 7 FDA reports)
RASH PUSTULAR ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
SCREAMING ( 7 FDA reports)
SEASONAL ALLERGY ( 7 FDA reports)
SECONDARY PROGRESSIVE MULTIPLE SCLEROSIS ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SYPHILIS ( 7 FDA reports)
URINARY HESITATION ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
VISUAL ACUITY REDUCED ( 7 FDA reports)
WHEELCHAIR USER ( 7 FDA reports)
WRIST FRACTURE ( 7 FDA reports)
ALCOHOL USE ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
BRUXISM ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CATHETER SITE SWELLING ( 6 FDA reports)
CORONARY ARTERY OCCLUSION ( 6 FDA reports)
DECUBITUS ULCER ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
EAR INFECTION ( 6 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
FACIAL ASYMMETRY ( 6 FDA reports)
FEELING DRUNK ( 6 FDA reports)
HIP ARTHROPLASTY ( 6 FDA reports)
HOSTILITY ( 6 FDA reports)
HYPOAESTHESIA ORAL ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
IMPAIRED WORK ABILITY ( 6 FDA reports)
JC VIRUS TEST POSITIVE ( 6 FDA reports)
JOINT LOCK ( 6 FDA reports)
MICTURITION URGENCY ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
POSTICTAL STATE ( 6 FDA reports)
RENAL MASS ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
SCRATCH ( 6 FDA reports)
SINUS DISORDER ( 6 FDA reports)
STRESS FRACTURE ( 6 FDA reports)
THERAPY CESSATION ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
TONIC CONVULSION ( 6 FDA reports)
WOUND ( 6 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
ASTHMA ( 5 FDA reports)
BAND SENSATION ( 5 FDA reports)
BLADDER PAIN ( 5 FDA reports)
BLOOD CALCIUM DECREASED ( 5 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
CERVICAL SPINAL STENOSIS ( 5 FDA reports)
CHOLECYSTITIS INFECTIVE ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
CLOSTRIDIAL INFECTION ( 5 FDA reports)
COMPLETED SUICIDE ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DRY EYE ( 5 FDA reports)
EAR DISCOMFORT ( 5 FDA reports)
FACE INJURY ( 5 FDA reports)
FORMICATION ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
INJECTION SITE NODULE ( 5 FDA reports)
INJECTION SITE REACTION ( 5 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 5 FDA reports)
INTESTINAL PERFORATION ( 5 FDA reports)
LIGAMENT RUPTURE ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
MIDDLE INSOMNIA ( 5 FDA reports)
MOOD SWINGS ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCLE RIGIDITY ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
NEUROGENIC BLADDER ( 5 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
RASH ERYTHEMATOUS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SIMPLE PARTIAL SEIZURES ( 5 FDA reports)
SKELETAL INJURY ( 5 FDA reports)
SKIN TURGOR DECREASED ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
VAGINAL DISCHARGE ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VIITH NERVE PARALYSIS ( 5 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 5 FDA reports)
WEIGHT BEARING DIFFICULTY ( 5 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
AGEUSIA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
APHAGIA ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
ARTHROPOD BITE ( 4 FDA reports)
BIPOLAR I DISORDER ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BRAIN INJURY ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COMPLEX PARTIAL SEIZURES ( 4 FDA reports)
DIZZINESS POSTURAL ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEELING JITTERY ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GASTROINTESTINAL INFECTION ( 4 FDA reports)
GASTROINTESTINAL VIRAL INFECTION ( 4 FDA reports)
GINGIVAL BLEEDING ( 4 FDA reports)
GINGIVAL BLISTER ( 4 FDA reports)
GINGIVAL PAIN ( 4 FDA reports)
GLOSSODYNIA ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
GRIP STRENGTH DECREASED ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEAD TITUBATION ( 4 FDA reports)
HEARING IMPAIRED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPERTONIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INJECTION SITE INFECTION ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
KLEBSIELLA BACTERAEMIA ( 4 FDA reports)
LIVER INJURY ( 4 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
LYME DISEASE ( 4 FDA reports)
MALIGNANT MELANOMA ( 4 FDA reports)
MANIA ( 4 FDA reports)
MENOPAUSE ( 4 FDA reports)
MULTIPLE FRACTURES ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OSTEOPENIA ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULMONARY THROMBOSIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SKIN INJURY ( 4 FDA reports)
SPINAL CORD DISORDER ( 4 FDA reports)
SPINAL DISORDER ( 4 FDA reports)
SURGERY ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
THIRST ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TIBIA FRACTURE ( 4 FDA reports)
TOXIC ENCEPHALOPATHY ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VISUAL FIELD DEFECT ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ACNE ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
ATRIAL FLUTTER ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BLOOD CALCIUM INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BRAIN OEDEMA ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
COLONIC STENOSIS ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
COMPULSIVE LIP BITING ( 3 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 3 FDA reports)
CYSTITIS KLEBSIELLA ( 3 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG PRESCRIBING ERROR ( 3 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 3 FDA reports)
DYSPHEMIA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
EMOTIONAL DISTRESS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FACIAL PAIN ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FIBULA FRACTURE ( 3 FDA reports)
FLUID INTAKE REDUCED ( 3 FDA reports)
FOAMING AT MOUTH ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FOOT DEFORMITY ( 3 FDA reports)
FUNGAL OESOPHAGITIS ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HEAT STROKE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYSTERECTOMY ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INCONTINENCE ( 3 FDA reports)
INFUSION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE CALCIFICATION ( 3 FDA reports)
INJECTION SITE CYST ( 3 FDA reports)
INJURY ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHOEDEMA ( 3 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
NASAL DRYNESS ( 3 FDA reports)
NECK INJURY ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
OESOPHAGEAL DISORDER ( 3 FDA reports)
OPTIC ATROPHY ( 3 FDA reports)
OPTIC NERVE DISORDER ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARANOIA ( 3 FDA reports)
PARAPARESIS ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PHARYNGEAL DISORDER ( 3 FDA reports)
PHOTOPHOBIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL ABSCESS ( 3 FDA reports)
REPETITIVE SPEECH ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SCAR ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENSORY LOSS ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SKIN HAEMORRHAGE ( 3 FDA reports)
SKIN IRRITATION ( 3 FDA reports)
SKULL FRACTURE ( 3 FDA reports)
SLUGGISHNESS ( 3 FDA reports)
SPINAL COLUMN STENOSIS ( 3 FDA reports)
SPONDYLITIS ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
TONGUE HAEMORRHAGE ( 3 FDA reports)
TOOTH INFECTION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TROPONIN T INCREASED ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGNOSIA ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANKLE OPERATION ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APRAXIA ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BENIGN RENAL NEOPLASM ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BREAST CANCER STAGE III ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
BUNION ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY ANEURYSM ( 2 FDA reports)
CELLULITIS ORBITAL ( 2 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
CHONDROPATHY ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CLONUS ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPARTMENT SYNDROME ( 2 FDA reports)
CONDUCTION DISORDER ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CYANOPSIA ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEATH OF PET ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE ISSUE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY THROAT ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE INJURY ( 2 FDA reports)
EYE ROLLING ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACIAL NEURALGIA ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FOREIGN BODY ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HEAD DEFORMITY ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEAT ILLNESS ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HORDEOLUM ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOPNOEA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INGROWING NAIL ( 2 FDA reports)
INJECTION SITE ATROPHY ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
JAW FRACTURE ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LOWER EXTREMITY MASS ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MALIGNANT MELANOMA STAGE II ( 2 FDA reports)
MARBURG'S VARIANT MULTIPLE SCLEROSIS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
METABOLIC DISORDER ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEURITIS ( 2 FDA reports)
NEUROGENIC SHOCK ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OPISTHOTONUS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PAINFUL DEFAECATION ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PARTIAL SEIZURES ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 2 FDA reports)
POLYMENORRHOEA ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROTEIN TOTAL INCREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RED BLOOD CELL MICROCYTES PRESENT ( 2 FDA reports)
RENAL CANCER ( 2 FDA reports)
RESIDUAL URINE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
ROTATOR CUFF REPAIR ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN CANDIDA ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN GRAFT ( 2 FDA reports)
SKIN TIGHTNESS ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SPINAL FUSION SURGERY ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
STERNAL FRACTURE ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TEETH BRITTLE ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TRANCE ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
UHTHOFF'S PHENOMENON ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS FLOATERS ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACQUIRED CLAW TOE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALLERGY TO ANIMAL ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANKLE DEFORMITY ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTIBODY TEST ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPLICATION SITE ATROPHY ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIARY NEOPLASM ( 1 FDA reports)
BILIARY TRACT OPERATION ( 1 FDA reports)
BILIRUBIN CONJUGATED ABNORMAL ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER CANCER STAGE III ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BORDERLINE GLAUCOMA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREAST CYST ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRUGADA SYNDROME ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURN INFECTION ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CARTILAGE ATROPHY ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL AUDITORY PROCESSING DISORDER ( 1 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL POLYP ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 1 FDA reports)
CORNEAL IMPLANT ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CRANIOCEREBRAL INJURY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYST ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE COMPONENT ISSUE ( 1 FDA reports)
DEVICE INVERSION ( 1 FDA reports)
DEVICE KINK ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DREAMY STATE ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSMORPHISM ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIC INFECTION ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENZYME ABNORMALITY ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ESCHERICHIA TEST POSITIVE ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 1 FDA reports)
FOOD AVERSION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREEZING PHENOMENON ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
FUNGAL SKIN INFECTION ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GAIT SPASTIC ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOCRIT ABNORMAL ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIANOPIA ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HERPES DERMATITIS ( 1 FDA reports)
HERPES SEPSIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIP SURGERY ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
JOINT HYPEREXTENSION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
JOINT WARMTH ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOARAIOSIS ( 1 FDA reports)
LHERMITTE'S SIGN ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIMB IMMOBILISATION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 1 FDA reports)
MEDICAL DEVICE PAIN ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGITIS VIRAL ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
METASTASES TO SALIVARY GLAND ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
MICTURITION FREQUENCY DECREASED ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OSCILLOPSIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
OVERCONFIDENCE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERIARTHRITIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PHARYNGEAL CYST ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREDISPOSITION TO DISEASE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRIMARY PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT SOLUBILITY ABNORMAL ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADICAL MASTECTOMY ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD INJURY LUMBAR ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STAB WOUND ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STICKY SKIN ( 1 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDON OPERATION ( 1 FDA reports)
TENSION ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID OPERATION ( 1 FDA reports)
TIC ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 1 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 1 FDA reports)
ULNAR NERVE INJURY ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URGE INCONTINENCE ( 1 FDA reports)
URINARY CYSTECTOMY ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE KETONE BODY ABSENT ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROSTOMY ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VENA CAVA THROMBOSIS ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VERBIGERATION ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VIBRATION TEST ABNORMAL ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

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