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

DEPRESSION ( 79 FDA reports)
HEADACHE ( 73 FDA reports)
OVERDOSE ( 68 FDA reports)
NAUSEA ( 64 FDA reports)
INSOMNIA ( 61 FDA reports)
ANXIETY ( 58 FDA reports)
FATIGUE ( 55 FDA reports)
PAIN ( 53 FDA reports)
SUICIDAL IDEATION ( 51 FDA reports)
DECREASED APPETITE ( 47 FDA reports)
WEIGHT DECREASED ( 46 FDA reports)
VOMITING ( 44 FDA reports)
CONVULSION ( 42 FDA reports)
DRUG INEFFECTIVE ( 42 FDA reports)
PULMONARY EMBOLISM ( 40 FDA reports)
DIZZINESS ( 38 FDA reports)
ABNORMAL BEHAVIOUR ( 36 FDA reports)
AGGRESSION ( 35 FDA reports)
FEELING ABNORMAL ( 35 FDA reports)
ABDOMINAL PAIN ( 34 FDA reports)
CHEST PAIN ( 34 FDA reports)
ABDOMINAL PAIN UPPER ( 33 FDA reports)
DYSPNOEA ( 33 FDA reports)
DRUG EFFECT DECREASED ( 31 FDA reports)
OFF LABEL USE ( 31 FDA reports)
ASTHENIA ( 29 FDA reports)
SOMNOLENCE ( 29 FDA reports)
HEART RATE INCREASED ( 28 FDA reports)
HALLUCINATION ( 27 FDA reports)
PYREXIA ( 27 FDA reports)
INJURY ( 26 FDA reports)
PAIN IN EXTREMITY ( 26 FDA reports)
TREMOR ( 26 FDA reports)
CONDITION AGGRAVATED ( 25 FDA reports)
FALL ( 25 FDA reports)
DISTURBANCE IN ATTENTION ( 24 FDA reports)
PSYCHOTIC DISORDER ( 24 FDA reports)
RASH ( 24 FDA reports)
WEIGHT INCREASED ( 24 FDA reports)
ARTHRALGIA ( 23 FDA reports)
BIPOLAR DISORDER ( 23 FDA reports)
GALLBLADDER DISORDER ( 23 FDA reports)
AGITATION ( 22 FDA reports)
COUGH ( 22 FDA reports)
PARAESTHESIA ( 22 FDA reports)
PRODUCT QUALITY ISSUE ( 22 FDA reports)
HYPOAESTHESIA ( 21 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 21 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 21 FDA reports)
ANGER ( 20 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 20 FDA reports)
BACK PAIN ( 19 FDA reports)
DEEP VEIN THROMBOSIS ( 19 FDA reports)
DIARRHOEA ( 19 FDA reports)
HYPERHIDROSIS ( 19 FDA reports)
IRRITABILITY ( 19 FDA reports)
MALAISE ( 19 FDA reports)
MOOD SWINGS ( 19 FDA reports)
TACHYCARDIA ( 19 FDA reports)
PALPITATIONS ( 18 FDA reports)
CHOLECYSTITIS CHRONIC ( 17 FDA reports)
SUICIDE ATTEMPT ( 17 FDA reports)
SYNCOPE ( 17 FDA reports)
ABDOMINAL DISTENSION ( 16 FDA reports)
TIC ( 16 FDA reports)
DRUG ABUSE ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 14 FDA reports)
CRYING ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
EMOTIONAL DISTRESS ( 14 FDA reports)
MOOD ALTERED ( 14 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 14 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 14 FDA reports)
AMNESIA ( 13 FDA reports)
CHILLS ( 13 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
DYSKINESIA ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
LYMPHADENOPATHY ( 13 FDA reports)
MUSCLE SPASMS ( 13 FDA reports)
PANIC ATTACK ( 13 FDA reports)
SLEEP DISORDER ( 13 FDA reports)
BILIARY DYSKINESIA ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
FEAR ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
INTENTIONAL OVERDOSE ( 12 FDA reports)
MIGRAINE ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
PARANOIA ( 12 FDA reports)
PLATELET COUNT DECREASED ( 12 FDA reports)
CLEFT PALATE ( 11 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
ROAD TRAFFIC ACCIDENT ( 11 FDA reports)
URINARY INCONTINENCE ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 10 FDA reports)
DRUG DEPENDENCE ( 10 FDA reports)
DRUG DIVERSION ( 10 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
IMPULSIVE BEHAVIOUR ( 10 FDA reports)
SINUSITIS ( 10 FDA reports)
TREATMENT NONCOMPLIANCE ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
CONJUNCTIVITIS ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
DRUG PRESCRIBING ERROR ( 9 FDA reports)
ECZEMA ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
INCORRECT DOSE ADMINISTERED ( 9 FDA reports)
INJECTION SITE PAIN ( 9 FDA reports)
LUNG NEOPLASM ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
PRESCRIBED OVERDOSE ( 9 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 9 FDA reports)
SKIN DISCOLOURATION ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BIOPSY BONE MARROW ( 8 FDA reports)
BIOPSY LYMPH GLAND ( 8 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 8 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
DRUG EFFECT INCREASED ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
EAR INFECTION ( 8 FDA reports)
ECZEMA EYELIDS ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
GRAND MAL CONVULSION ( 8 FDA reports)
HALLUCINATION, AUDITORY ( 8 FDA reports)
MASS EXCISION ( 8 FDA reports)
MENTAL DISORDER ( 8 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 8 FDA reports)
MUSCULOSKELETAL PAIN ( 8 FDA reports)
NECK PAIN ( 8 FDA reports)
PLATELET COUNT INCREASED ( 8 FDA reports)
REFLUX OESOPHAGITIS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SPLENOMEGALY ( 8 FDA reports)
THROMBOSIS ( 8 FDA reports)
TOE WALKING ( 8 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 8 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
VIRAL PHARYNGITIS ( 8 FDA reports)
ABDOMINAL DISCOMFORT ( 7 FDA reports)
ABDOMINAL PAIN LOWER ( 7 FDA reports)
AFFECT LABILITY ( 7 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 7 FDA reports)
BRONCHITIS ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
CROHN'S DISEASE ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
GALLBLADDER INJURY ( 7 FDA reports)
HOMICIDAL IDEATION ( 7 FDA reports)
ILEAL STENOSIS ( 7 FDA reports)
IMPAIRED WORK ABILITY ( 7 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 7 FDA reports)
INTESTINAL FISTULA ( 7 FDA reports)
INTESTINAL OBSTRUCTION ( 7 FDA reports)
MUSCLE STRAIN ( 7 FDA reports)
NEUTROPHIL COUNT INCREASED ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PELVIC PAIN ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 7 FDA reports)
TARDIVE DYSKINESIA ( 7 FDA reports)
TYPE 1 DIABETES MELLITUS ( 7 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 6 FDA reports)
ADVERSE EVENT ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
DIPLOPIA ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
EDUCATIONAL PROBLEM ( 6 FDA reports)
EMOTIONAL DISORDER ( 6 FDA reports)
FLUSHING ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HYPERCOAGULATION ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
INJECTION SITE ERYTHEMA ( 6 FDA reports)
INJECTION SITE HAEMORRHAGE ( 6 FDA reports)
MULTIPLE INJURIES ( 6 FDA reports)
NERVE INJURY ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
NIGHTMARE ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PHYSICAL ASSAULT ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
PULMONARY INFARCTION ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
STRESS ( 6 FDA reports)
SUDDEN DEATH ( 6 FDA reports)
THINKING ABNORMAL ( 6 FDA reports)
TYPE 2 DIABETES MELLITUS ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VITAMIN D DEFICIENCY ( 6 FDA reports)
ARTHRITIS ( 5 FDA reports)
AUTISM SPECTRUM DISORDER ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CANDIDIASIS ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DRUG ABUSER ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
DRUG SCREEN POSITIVE ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
FUNGAL INFECTION ( 5 FDA reports)
GASTRIC DISORDER ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
IMPULSE-CONTROL DISORDER ( 5 FDA reports)
INFLUENZA LIKE ILLNESS ( 5 FDA reports)
INTENTIONAL DRUG MISUSE ( 5 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
JOINT SWELLING ( 5 FDA reports)
MANIA ( 5 FDA reports)
MUSCLE TWITCHING ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PROCEDURAL COMPLICATION ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SENSORY DISTURBANCE ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
SWELLING ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
UPPER LIMB FRACTURE ( 5 FDA reports)
VAGINAL HAEMORRHAGE ( 5 FDA reports)
VIRAL INFECTION ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 5 FDA reports)
ABNORMAL DREAMS ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
ADNEXA UTERI PAIN ( 4 FDA reports)
AFFECTIVE DISORDER ( 4 FDA reports)
ANAEMIA ( 4 FDA reports)
ANXIETY DISORDER ( 4 FDA reports)
APATHY ( 4 FDA reports)
APHASIA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
AUTOIMMUNE THYROIDITIS ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BASEDOW'S DISEASE ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC MURMUR ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CARDIOMYOPATHY ( 4 FDA reports)
CHOLECYSTITIS ACUTE ( 4 FDA reports)
COMA ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 4 FDA reports)
FLAT AFFECT ( 4 FDA reports)
FLATULENCE ( 4 FDA reports)
FLIGHT OF IDEAS ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GOUT ( 4 FDA reports)
GROWTH RETARDATION ( 4 FDA reports)
GUN SHOT WOUND ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOMANIA ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MUSCLE TIGHTNESS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OVARIAN CYST ( 4 FDA reports)
PANCREATITIS ACUTE ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RAYNAUD'S PHENOMENON ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESPIRATORY RATE INCREASED ( 4 FDA reports)
SINUS HEADACHE ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
SOCIAL PROBLEM ( 4 FDA reports)
SUDDEN CARDIAC DEATH ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 4 FDA reports)
THIRST DECREASED ( 4 FDA reports)
THROAT IRRITATION ( 4 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UNINTENDED PREGNANCY ( 4 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 4 FDA reports)
VISUAL ACUITY REDUCED ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACCIDENT ( 3 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 3 FDA reports)
ADHESION ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANTISOCIAL BEHAVIOUR ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CEREBRAL ISCHAEMIA ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
CRIME ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEVICE DISLOCATION ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
DRUG DISPENSING ERROR ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
ENERGY INCREASED ( 3 FDA reports)
EXOPHTHALMOS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOOT FRACTURE ( 3 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATITIS C ( 3 FDA reports)
HIP ARTHROPLASTY ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPERTONIC BLADDER ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE NODULE ( 3 FDA reports)
INTENTIONAL SELF-INJURY ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
JAW FRACTURE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LOCAL SWELLING ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MUSCLE ATROPHY ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NARCOLEPSY ( 3 FDA reports)
OBESITY ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POSTPARTUM DEPRESSION ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATOMEGALY ( 3 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RETCHING ( 3 FDA reports)
ROCKY MOUNTAIN SPOTTED FEVER ( 3 FDA reports)
SCAR ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SEDATION ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SEXUAL ABUSE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SLEEP TERROR ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
SUICIDAL BEHAVIOUR ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
URINE AMPHETAMINE POSITIVE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABDOMEN CRUSHING ( 2 FDA reports)
ACCIDENT AT WORK ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE SINUSITIS ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ARTERIOSPASM CORONARY ( 2 FDA reports)
ASTHENOPIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AUTISM ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
BACTERIAL TOXAEMIA ( 2 FDA reports)
BIOPSY ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
CARBON MONOXIDE POISONING ( 2 FDA reports)
CAROTID ARTERY DISSECTION ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLONIC STENOSIS ( 2 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSOCIATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSMENORRHOEA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ENDOMETRITIS DECIDUAL ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FACIAL NERVE DISORDER ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
GALLBLADDER ENLARGEMENT ( 2 FDA reports)
GALLBLADDER PAIN ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INCISION SITE PAIN ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
IRREGULAR SLEEP PHASE ( 2 FDA reports)
JOINT STIFFNESS ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
KNEE OPERATION ( 2 FDA reports)
LACRIMATION INCREASED ( 2 FDA reports)
LEGAL PROBLEM ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIBIDO DECREASED ( 2 FDA reports)
LIMB CRUSHING INJURY ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MEDICATION TAMPERING ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MYOCARDITIS BACTERIAL ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEURALGIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IIIA ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPEN WOUND ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAINFUL RESPIRATION ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PELVIC FRACTURE ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PLEURAL FIBROSIS ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 2 FDA reports)
POSTURE ABNORMAL ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL PROLAPSE ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RETINAL TEAR ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TESTICULAR INJURY ( 2 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX DECREASED ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE URIC ACID INCREASED ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENOUS INSUFFICIENCY ( 2 FDA reports)
VICTIM OF CRIME ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMPHETAMINES NEGATIVE ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE ECZEMA ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE FREE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN DAMAGE ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CAPSULE PHYSICAL ISSUE ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBROVASCULAR ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
CHANGE IN SUSTAINED ATTENTION ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCT DISORDER ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONSTRICTED AFFECT ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS ATOPIC ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIZZINESS EXERTIONAL ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPAREUNIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE EYE BLINKING ( 1 FDA reports)
EXCESSIVE MASTURBATION ( 1 FDA reports)
EXERCISE LACK OF ( 1 FDA reports)
EXHIBITIONISM ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO COMMUNICABLE DISEASE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACTOR V LEIDEN MUTATION ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIGHT IN SCHOOL ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GALLBLADDER OPERATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERINSULINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MATERNAL EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METAL POISONING ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE III ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR NEOPLASM ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARATHYROID DISORDER ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHOBIA OF DRIVING ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 1 FDA reports)
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME ( 1 FDA reports)
PRECOCIOUS PUBERTY ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PRODUCT TASTE ABNORMAL ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 1 FDA reports)
PSYCHIATRIC SYMPTOM ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
REGRESSIVE BEHAVIOUR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 1 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCHOOL REFUSAL ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SKIN PAPILLOMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL FRACTURE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SLEEP-RELATED EATING DISORDER ( 1 FDA reports)
SOCIAL FEAR ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPUTUM ABNORMAL ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SUTURE RUPTURE ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYRINGOMYELIA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRAUMATIC BRAIN INJURY ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UNWANTED PREGNANCY ( 1 FDA reports)
UTERINE PAIN ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOUS INJURY ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VICTIM OF SPOUSAL ABUSE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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