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

DRUG INEFFECTIVE ( 396 FDA reports)
CONDITION AGGRAVATED ( 199 FDA reports)
PAIN ( 193 FDA reports)
DIZZINESS ( 177 FDA reports)
FEELING ABNORMAL ( 159 FDA reports)
ASTHENIA ( 153 FDA reports)
SOMNOLENCE ( 153 FDA reports)
PAIN IN EXTREMITY ( 131 FDA reports)
INSOMNIA ( 130 FDA reports)
DEPRESSION ( 128 FDA reports)
HEADACHE ( 128 FDA reports)
WEIGHT DECREASED ( 127 FDA reports)
HYPERTENSION ( 126 FDA reports)
DYSPNOEA ( 120 FDA reports)
NAUSEA ( 120 FDA reports)
MYOCARDIAL INFARCTION ( 119 FDA reports)
DRUG INTERACTION ( 117 FDA reports)
FATIGUE ( 116 FDA reports)
WEIGHT INCREASED ( 113 FDA reports)
VOMITING ( 112 FDA reports)
SUICIDE ATTEMPT ( 107 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 106 FDA reports)
FALL ( 106 FDA reports)
ANXIETY ( 103 FDA reports)
OEDEMA PERIPHERAL ( 102 FDA reports)
CEREBROVASCULAR ACCIDENT ( 101 FDA reports)
CONVULSION ( 101 FDA reports)
DIARRHOEA ( 101 FDA reports)
TREATMENT NONCOMPLIANCE ( 99 FDA reports)
DIFFICULTY IN WALKING ( 93 FDA reports)
ARTHRALGIA ( 89 FDA reports)
MALAISE ( 88 FDA reports)
TREMOR ( 87 FDA reports)
LOSS OF CONSCIOUSNESS ( 85 FDA reports)
COMPLETED SUICIDE ( 84 FDA reports)
CHEST PAIN ( 83 FDA reports)
MYALGIA ( 80 FDA reports)
BACK PAIN ( 77 FDA reports)
MUSCLE SPASMS ( 72 FDA reports)
RASH ( 72 FDA reports)
VISION BLURRED ( 72 FDA reports)
BLOOD PRESSURE INCREASED ( 71 FDA reports)
DRUG EFFECT DECREASED ( 70 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 65 FDA reports)
HYPOAESTHESIA ( 64 FDA reports)
OVERDOSE ( 64 FDA reports)
GAIT DISTURBANCE ( 63 FDA reports)
ARTHRITIS ( 60 FDA reports)
CONSTIPATION ( 60 FDA reports)
MEMORY IMPAIRMENT ( 59 FDA reports)
CARDIAC ARREST ( 58 FDA reports)
DIABETES MELLITUS ( 58 FDA reports)
CARDIAC DISORDER ( 57 FDA reports)
CARDIAC FAILURE ( 56 FDA reports)
BALANCE DISORDER ( 55 FDA reports)
ABDOMINAL PAIN UPPER ( 54 FDA reports)
CONFUSIONAL STATE ( 54 FDA reports)
AMNESIA ( 53 FDA reports)
BLOOD GLUCOSE INCREASED ( 53 FDA reports)
DEHYDRATION ( 53 FDA reports)
BODY HEIGHT DECREASED ( 52 FDA reports)
HYPERSENSITIVITY ( 52 FDA reports)
MULTIPLE DRUG OVERDOSE ( 51 FDA reports)
PNEUMONIA ( 51 FDA reports)
PYREXIA ( 51 FDA reports)
VISUAL DISTURBANCE ( 51 FDA reports)
DRY MOUTH ( 49 FDA reports)
PARAESTHESIA ( 48 FDA reports)
CORONARY ARTERY OCCLUSION ( 47 FDA reports)
DRUG HYPERSENSITIVITY ( 47 FDA reports)
RHABDOMYOLYSIS ( 47 FDA reports)
ANOREXIA ( 46 FDA reports)
ATRIAL FIBRILLATION ( 46 FDA reports)
POST PROCEDURAL COMPLICATION ( 46 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 45 FDA reports)
RESPIRATORY ARREST ( 45 FDA reports)
URINARY TRACT INFECTION ( 45 FDA reports)
CATARACT ( 44 FDA reports)
COMA ( 44 FDA reports)
DRUG TOXICITY ( 44 FDA reports)
HEART RATE INCREASED ( 44 FDA reports)
INTENTIONAL MISUSE ( 44 FDA reports)
MUSCULAR WEAKNESS ( 44 FDA reports)
ABASIA ( 43 FDA reports)
ABDOMINAL PAIN ( 43 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 43 FDA reports)
ANAEMIA ( 42 FDA reports)
INCORRECT DOSE ADMINISTERED ( 41 FDA reports)
AGGRESSION ( 40 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 40 FDA reports)
PRURITUS ( 40 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 40 FDA reports)
HAEMOGLOBIN DECREASED ( 39 FDA reports)
HYPOTENSION ( 39 FDA reports)
RENAL FAILURE ACUTE ( 39 FDA reports)
SPEECH DISORDER ( 39 FDA reports)
URTICARIA ( 39 FDA reports)
RENAL FAILURE ( 38 FDA reports)
SUICIDAL IDEATION ( 37 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 36 FDA reports)
DISORIENTATION ( 36 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 36 FDA reports)
INFECTION ( 36 FDA reports)
MEDICATION ERROR ( 36 FDA reports)
SLEEP DISORDER ( 36 FDA reports)
AGITATION ( 35 FDA reports)
COUGH ( 35 FDA reports)
NECK PAIN ( 35 FDA reports)
NERVOUSNESS ( 34 FDA reports)
PLATELET COUNT DECREASED ( 34 FDA reports)
UNEVALUABLE EVENT ( 34 FDA reports)
VISUAL ACUITY REDUCED ( 34 FDA reports)
IRRITABILITY ( 33 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 33 FDA reports)
OSTEOARTHRITIS ( 33 FDA reports)
THERAPY NON-RESPONDER ( 33 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 32 FDA reports)
BLOOD CREATININE INCREASED ( 32 FDA reports)
CONTUSION ( 32 FDA reports)
DYSPEPSIA ( 32 FDA reports)
HYPOKALAEMIA ( 32 FDA reports)
MENTAL DISORDER ( 32 FDA reports)
ROAD TRAFFIC ACCIDENT ( 32 FDA reports)
TACHYCARDIA ( 32 FDA reports)
HAEMORRHAGE ( 31 FDA reports)
HYPERHIDROSIS ( 31 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 30 FDA reports)
BLOOD PRESSURE DECREASED ( 30 FDA reports)
BURNING SENSATION ( 30 FDA reports)
CHEST DISCOMFORT ( 30 FDA reports)
DISEASE RECURRENCE ( 30 FDA reports)
DYSPHAGIA ( 30 FDA reports)
ERYTHEMA ( 30 FDA reports)
OSTEOPOROSIS ( 30 FDA reports)
PALPITATIONS ( 30 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 29 FDA reports)
STOMACH DISCOMFORT ( 29 FDA reports)
ALOPECIA ( 28 FDA reports)
DYSSTASIA ( 28 FDA reports)
RENAL DISORDER ( 28 FDA reports)
STAPHYLOCOCCAL INFECTION ( 28 FDA reports)
SWELLING ( 28 FDA reports)
VERTIGO ( 28 FDA reports)
DIALYSIS ( 27 FDA reports)
DISTURBANCE IN ATTENTION ( 27 FDA reports)
INJURY ( 27 FDA reports)
NERVE INJURY ( 27 FDA reports)
SYNCOPE ( 27 FDA reports)
ABNORMAL BEHAVIOUR ( 26 FDA reports)
BLINDNESS ( 26 FDA reports)
EYE DISORDER ( 26 FDA reports)
NEUROPATHY ( 26 FDA reports)
SEPSIS ( 26 FDA reports)
ASTHMA ( 25 FDA reports)
BLOOD SODIUM DECREASED ( 25 FDA reports)
CRYING ( 25 FDA reports)
DYSARTHRIA ( 25 FDA reports)
FLUID RETENTION ( 25 FDA reports)
GASTROINTESTINAL DISORDER ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
ERECTILE DYSFUNCTION ( 24 FDA reports)
FLATULENCE ( 24 FDA reports)
HYPOGLYCAEMIA ( 24 FDA reports)
NERVOUS SYSTEM DISORDER ( 24 FDA reports)
PSYCHOTIC DISORDER ( 24 FDA reports)
SKIN DISCOLOURATION ( 24 FDA reports)
STRESS ( 24 FDA reports)
ARRHYTHMIA ( 23 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
DYSKINESIA ( 23 FDA reports)
HAEMATOCRIT DECREASED ( 23 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 23 FDA reports)
THROMBOSIS ( 23 FDA reports)
BLOOD POTASSIUM DECREASED ( 22 FDA reports)
CYSTITIS ( 22 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 22 FDA reports)
ECONOMIC PROBLEM ( 22 FDA reports)
HALLUCINATION ( 22 FDA reports)
INFLAMMATION ( 22 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
MOVEMENT DISORDER ( 22 FDA reports)
NASOPHARYNGITIS ( 22 FDA reports)
SWELLING FACE ( 22 FDA reports)
BRADYCARDIA ( 21 FDA reports)
KNEE ARTHROPLASTY ( 21 FDA reports)
OEDEMA ( 21 FDA reports)
PROSTATE CANCER ( 21 FDA reports)
URINARY INCONTINENCE ( 21 FDA reports)
ARTHROPATHY ( 20 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 20 FDA reports)
INTENTIONAL OVERDOSE ( 20 FDA reports)
MUSCLE DISORDER ( 20 FDA reports)
PARANOIA ( 20 FDA reports)
SURGERY ( 20 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 20 FDA reports)
BLOOD BILIRUBIN INCREASED ( 19 FDA reports)
CARDIAC OPERATION ( 19 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 19 FDA reports)
DRUG DEPENDENCE ( 19 FDA reports)
GLAUCOMA ( 19 FDA reports)
HIP ARTHROPLASTY ( 19 FDA reports)
HYPERSOMNIA ( 19 FDA reports)
MACULAR DEGENERATION ( 19 FDA reports)
NEURALGIA ( 19 FDA reports)
ORAL INTAKE REDUCED ( 19 FDA reports)
SINUSITIS ( 19 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
DISEASE PROGRESSION ( 18 FDA reports)
FEELING COLD ( 18 FDA reports)
GASTRIC DISORDER ( 18 FDA reports)
IMPAIRED DRIVING ABILITY ( 18 FDA reports)
MIGRAINE ( 18 FDA reports)
MYOCARDIAL ISCHAEMIA ( 18 FDA reports)
PANCREATITIS ( 18 FDA reports)
PANIC ATTACK ( 18 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
SEDATION ( 18 FDA reports)
THINKING ABNORMAL ( 18 FDA reports)
ABDOMINAL DISTENSION ( 17 FDA reports)
ANGER ( 17 FDA reports)
ANGINA PECTORIS ( 17 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 17 FDA reports)
DYSGEUSIA ( 17 FDA reports)
FLUSHING ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
INADEQUATE ANALGESIA ( 17 FDA reports)
INCONTINENCE ( 17 FDA reports)
INTENTIONAL DRUG MISUSE ( 17 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 17 FDA reports)
LETHARGY ( 17 FDA reports)
NEUROPATHY PERIPHERAL ( 17 FDA reports)
POLLAKIURIA ( 17 FDA reports)
SCAR ( 17 FDA reports)
BLOOD URINE PRESENT ( 16 FDA reports)
CORONARY ARTERY DISEASE ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
DELIRIUM ( 16 FDA reports)
DYSURIA ( 16 FDA reports)
EPILEPSY ( 16 FDA reports)
EYE SWELLING ( 16 FDA reports)
FEELING HOT ( 16 FDA reports)
FIBROMYALGIA ( 16 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 16 FDA reports)
HYPONATRAEMIA ( 16 FDA reports)
IMPAIRED HEALING ( 16 FDA reports)
IMPAIRED WORK ABILITY ( 16 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 16 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 16 FDA reports)
MUSCLE ATROPHY ( 16 FDA reports)
SPINAL COLUMN STENOSIS ( 16 FDA reports)
STEVENS-JOHNSON SYNDROME ( 16 FDA reports)
VENTRICULAR TACHYCARDIA ( 16 FDA reports)
VIRAL INFECTION ( 16 FDA reports)
BACK DISORDER ( 15 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 15 FDA reports)
DIPLOPIA ( 15 FDA reports)
EMOTIONAL DISORDER ( 15 FDA reports)
EUPHORIC MOOD ( 15 FDA reports)
EYE HAEMORRHAGE ( 15 FDA reports)
HEAD INJURY ( 15 FDA reports)
HEPATIC FAILURE ( 15 FDA reports)
JOINT SWELLING ( 15 FDA reports)
PULMONARY OEDEMA ( 15 FDA reports)
RASH ERYTHEMATOUS ( 15 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 15 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 15 FDA reports)
RESTLESSNESS ( 15 FDA reports)
SHOULDER PAIN ( 15 FDA reports)
SUDDEN DEATH ( 15 FDA reports)
TINNITUS ( 15 FDA reports)
APHASIA ( 14 FDA reports)
BLINDNESS UNILATERAL ( 14 FDA reports)
BLISTER ( 14 FDA reports)
BLOOD CHLORIDE DECREASED ( 14 FDA reports)
BLOOD POTASSIUM INCREASED ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 14 FDA reports)
BONE PAIN ( 14 FDA reports)
CELLULITIS ( 14 FDA reports)
EYE PAIN ( 14 FDA reports)
FEAR ( 14 FDA reports)
GASTRIC ULCER ( 14 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 14 FDA reports)
GRAND MAL CONVULSION ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
HEPATIC ENZYME INCREASED ( 14 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 14 FDA reports)
MUSCULOSKELETAL PAIN ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
ANGIONEUROTIC OEDEMA ( 13 FDA reports)
BIPOLAR DISORDER ( 13 FDA reports)
BLOOD DISORDER ( 13 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
CHILLS ( 13 FDA reports)
DRUG INTOLERANCE ( 13 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 13 FDA reports)
GASTRITIS ( 13 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 13 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
SURGICAL PROCEDURE REPEATED ( 13 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 13 FDA reports)
TORSADE DE POINTES ( 13 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
VISUAL FIELD DEFECT ( 13 FDA reports)
ANAESTHETIC COMPLICATION ( 12 FDA reports)
CARDIOVASCULAR DISORDER ( 12 FDA reports)
COGNITIVE DISORDER ( 12 FDA reports)
DISCOMFORT ( 12 FDA reports)
DRUG ABUSER ( 12 FDA reports)
DRUG DOSE OMISSION ( 12 FDA reports)
EPISTAXIS ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
FACIAL PAIN ( 12 FDA reports)
GASTRIC HAEMORRHAGE ( 12 FDA reports)
GENERALISED OEDEMA ( 12 FDA reports)
HAEMODIALYSIS ( 12 FDA reports)
HEART RATE DECREASED ( 12 FDA reports)
HYPOKINESIA ( 12 FDA reports)
INTENTIONAL SELF-INJURY ( 12 FDA reports)
MICTURITION URGENCY ( 12 FDA reports)
MYOPATHY ( 12 FDA reports)
NEPHROLITHIASIS ( 12 FDA reports)
NIGHTMARE ( 12 FDA reports)
PLATELET COUNT INCREASED ( 12 FDA reports)
PROTHROMBIN TIME PROLONGED ( 12 FDA reports)
SELF-MEDICATION ( 12 FDA reports)
SKIN EXFOLIATION ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
URINARY RETENTION ( 12 FDA reports)
ADVERSE EVENT ( 11 FDA reports)
ALCOHOL USE ( 11 FDA reports)
ANURIA ( 11 FDA reports)
BEDRIDDEN ( 11 FDA reports)
BRONCHITIS ( 11 FDA reports)
CEREBRAL HAEMORRHAGE ( 11 FDA reports)
COORDINATION ABNORMAL ( 11 FDA reports)
DEAFNESS ( 11 FDA reports)
EATING DISORDER ( 11 FDA reports)
GINGIVAL PAIN ( 11 FDA reports)
HEART RATE IRREGULAR ( 11 FDA reports)
INFLUENZA LIKE ILLNESS ( 11 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 11 FDA reports)
JAUNDICE ( 11 FDA reports)
LIMB INJURY ( 11 FDA reports)
MOBILITY DECREASED ( 11 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
MUSCLE CRAMP ( 11 FDA reports)
MUSCLE TWITCHING ( 11 FDA reports)
PARALYSIS ( 11 FDA reports)
PHOTOPHOBIA ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
PROCEDURAL COMPLICATION ( 11 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 11 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 11 FDA reports)
SENSATION OF HEAVINESS ( 11 FDA reports)
SENSORY LOSS ( 11 FDA reports)
SEXUAL DYSFUNCTION ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
ACCIDENT ( 10 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
BREAST CANCER ( 10 FDA reports)
CANDIDIASIS ( 10 FDA reports)
DEATH ( 10 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 10 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 10 FDA reports)
DRUG DISPENSING ERROR ( 10 FDA reports)
DRUG LEVEL INCREASED ( 10 FDA reports)
EYE IRRITATION ( 10 FDA reports)
GUN SHOT WOUND ( 10 FDA reports)
HAEMATEMESIS ( 10 FDA reports)
HIP FRACTURE ( 10 FDA reports)
INJECTION SITE PAIN ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
PAIN IN JAW ( 10 FDA reports)
PHARYNGEAL OEDEMA ( 10 FDA reports)
PNEUMONIA ASPIRATION ( 10 FDA reports)
PULMONARY EMBOLISM ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
SENSORY DISTURBANCE ( 10 FDA reports)
SLEEP APNOEA SYNDROME ( 10 FDA reports)
ULCER ( 10 FDA reports)
VASCULAR BYPASS GRAFT ( 10 FDA reports)
ACNE ( 9 FDA reports)
ANAPHYLACTIC REACTION ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 9 FDA reports)
BLOOD GLUCOSE DECREASED ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
BURSITIS ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CARDIAC PACEMAKER INSERTION ( 9 FDA reports)
COLITIS ( 9 FDA reports)
CORONARY ARTERY SURGERY ( 9 FDA reports)
DIABETIC NEUROPATHY ( 9 FDA reports)
EJECTION FRACTION DECREASED ( 9 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 9 FDA reports)
EMPHYSEMA ( 9 FDA reports)
FEELING DRUNK ( 9 FDA reports)
FEELING JITTERY ( 9 FDA reports)
GLOSSODYNIA ( 9 FDA reports)
HEPATITIS ( 9 FDA reports)
HEPATITIS FULMINANT ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
ILL-DEFINED DISORDER ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
INTESTINAL OBSTRUCTION ( 9 FDA reports)
KNEE OPERATION ( 9 FDA reports)
MENTAL STATUS CHANGES ( 9 FDA reports)
MIDDLE INSOMNIA ( 9 FDA reports)
MOOD ALTERED ( 9 FDA reports)
MULTIPLE ALLERGIES ( 9 FDA reports)
NOCTURIA ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RETCHING ( 9 FDA reports)
SEPTIC SHOCK ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
SPINAL DISORDER ( 9 FDA reports)
STENT PLACEMENT ( 9 FDA reports)
STRESS SYMPTOMS ( 9 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 9 FDA reports)
TENDERNESS ( 9 FDA reports)
THROAT IRRITATION ( 9 FDA reports)
THYROID DISORDER ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 9 FDA reports)
WALKING AID USER ( 9 FDA reports)
WEIGHT FLUCTUATION ( 9 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
ASCITES ( 8 FDA reports)
AURA ( 8 FDA reports)
BACTERIAL INFECTION ( 8 FDA reports)
BLADDER DISORDER ( 8 FDA reports)
BLOOD PRESSURE ABNORMAL ( 8 FDA reports)
BLOOD SODIUM INCREASED ( 8 FDA reports)
BREAST CANCER FEMALE ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CARPAL TUNNEL SYNDROME ( 8 FDA reports)
COAGULOPATHY ( 8 FDA reports)
CORONARY ARTERY STENOSIS ( 8 FDA reports)
DECREASED ACTIVITY ( 8 FDA reports)
DEMENTIA ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DRY SKIN ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
ERECTION INCREASED ( 8 FDA reports)
EYE PRURITUS ( 8 FDA reports)
FUNGAL INFECTION ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
HAEMATOMA ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HERNIA ( 8 FDA reports)
HIATUS HERNIA ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPERTENSIVE CRISIS ( 8 FDA reports)
INCOHERENT ( 8 FDA reports)
INFLUENZA ( 8 FDA reports)
LIBIDO DECREASED ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
LUNG NEOPLASM MALIGNANT ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MELAENA ( 8 FDA reports)
METASTASES TO LIVER ( 8 FDA reports)
MULTIPLE SCLEROSIS ( 8 FDA reports)
MYOCLONUS ( 8 FDA reports)
NASAL CONGESTION ( 8 FDA reports)
NECK INJURY ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
POLYMYOSITIS ( 8 FDA reports)
POST PROCEDURAL NAUSEA ( 8 FDA reports)
PROTEIN URINE PRESENT ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
RENAL PAIN ( 8 FDA reports)
RESPIRATORY DEPRESSION ( 8 FDA reports)
SCREAMING ( 8 FDA reports)
SHOCK ( 8 FDA reports)
SINUS DISORDER ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
THERMAL BURN ( 8 FDA reports)
ULCER HAEMORRHAGE ( 8 FDA reports)
VAGINAL HAEMORRHAGE ( 8 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 7 FDA reports)
ALCOHOLISM ( 7 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
ANKLE FRACTURE ( 7 FDA reports)
AORTIC ANEURYSM ( 7 FDA reports)
BACK INJURY ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CARDIOMYOPATHY ( 7 FDA reports)
CEREBROVASCULAR DISORDER ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
EJACULATION DISORDER ( 7 FDA reports)
FAECAL INCONTINENCE ( 7 FDA reports)
FOOD INTERACTION ( 7 FDA reports)
FOOT FRACTURE ( 7 FDA reports)
HAEMOPTYSIS ( 7 FDA reports)
HEMIPARESIS ( 7 FDA reports)
HEPATOMEGALY ( 7 FDA reports)
HOSTILITY ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HYPOTHERMIA ( 7 FDA reports)
IATROGENIC INJURY ( 7 FDA reports)
LABORATORY TEST ABNORMAL ( 7 FDA reports)
LACRIMATION INCREASED ( 7 FDA reports)
LACTIC ACIDOSIS ( 7 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 7 FDA reports)
MENOPAUSE ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
MYOSITIS ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
NODULE ( 7 FDA reports)
OCULAR VASCULAR DISORDER ( 7 FDA reports)
OPTIC NERVE DISORDER ( 7 FDA reports)
ORAL CANDIDIASIS ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PERIPHERAL COLDNESS ( 7 FDA reports)
PHOTOSENSITIVITY REACTION ( 7 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 7 FDA reports)
PROCEDURAL PAIN ( 7 FDA reports)
RASH MACULAR ( 7 FDA reports)
RASH PAPULAR ( 7 FDA reports)
RECTAL HAEMORRHAGE ( 7 FDA reports)
RESTLESS LEGS SYNDROME ( 7 FDA reports)
SCIATICA ( 7 FDA reports)
SINUS BRADYCARDIA ( 7 FDA reports)
SKIN LACERATION ( 7 FDA reports)
SKIN LESION ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
VENTRICULAR HYPERTROPHY ( 7 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 7 FDA reports)
ABDOMINAL DISCOMFORT ( 6 FDA reports)
ABNORMAL DREAMS ( 6 FDA reports)
ACTINIC KERATOSIS ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANGIOPATHY ( 6 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 6 FDA reports)
BIPOLAR I DISORDER ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 6 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
CEREBRAL INFARCTION ( 6 FDA reports)
CHOLESTASIS ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DENTAL CARIES ( 6 FDA reports)
DIVERTICULUM ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
EYELID PTOSIS ( 6 FDA reports)
FACIAL PALSY ( 6 FDA reports)
FORMICATION ( 6 FDA reports)
GALACTORRHOEA ( 6 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 6 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 6 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 6 FDA reports)
GOUT ( 6 FDA reports)
HALLUCINATION, AUDITORY ( 6 FDA reports)
HEARING IMPAIRED ( 6 FDA reports)
HEPATIC CIRRHOSIS ( 6 FDA reports)
HEPATITIS GRANULOMATOUS ( 6 FDA reports)
HEPATOCELLULAR DAMAGE ( 6 FDA reports)
HERNIA REPAIR ( 6 FDA reports)
HYPOACUSIS ( 6 FDA reports)
HYPOREFLEXIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 6 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 6 FDA reports)
KYPHOSIS ( 6 FDA reports)
LOCALISED OSTEOARTHRITIS ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LOSS OF CONTROL OF LEGS ( 6 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MANIA ( 6 FDA reports)
MEDICAL DEVICE COMPLICATION ( 6 FDA reports)
METRORRHAGIA ( 6 FDA reports)
MITRAL VALVE PROLAPSE ( 6 FDA reports)
MOOD SWINGS ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 6 FDA reports)
NECROSIS ( 6 FDA reports)
OESOPHAGEAL SPASM ( 6 FDA reports)
PARKINSON'S DISEASE ( 6 FDA reports)
PERSONALITY CHANGE ( 6 FDA reports)
POISONING ( 6 FDA reports)
POLYTRAUMATISM ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
POSTURE ABNORMAL ( 6 FDA reports)
PSEUDOMONAS INFECTION ( 6 FDA reports)
RADICULOPATHY ( 6 FDA reports)
RECTAL POLYP ( 6 FDA reports)
RESPIRATORY DISTRESS ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
RETINAL HAEMORRHAGE ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
ROTATOR CUFF SYNDROME ( 6 FDA reports)
SCAB ( 6 FDA reports)
SKIN HAEMORRHAGE ( 6 FDA reports)
SPINAL COMPRESSION FRACTURE ( 6 FDA reports)
SPINAL OPERATION ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
TARDIVE DYSKINESIA ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 6 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
VASODILATATION ( 6 FDA reports)
VITREOUS FLOATERS ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABORTION ( 5 FDA reports)
ABSCESS ( 5 FDA reports)
ANGINA UNSTABLE ( 5 FDA reports)
AORTIC VALVE INCOMPETENCE ( 5 FDA reports)
ASPIRATION ( 5 FDA reports)
BLINDNESS TRANSIENT ( 5 FDA reports)
BLOOD URINE ( 5 FDA reports)
BLOODY DISCHARGE ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CALCINOSIS ( 5 FDA reports)
CARDIAC VALVE DISEASE ( 5 FDA reports)
CAROTID ARTERY STENOSIS ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
CONCUSSION ( 5 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
CYSTITIS INTERSTITIAL ( 5 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 5 FDA reports)
DRUG LEVEL DECREASED ( 5 FDA reports)
DRUG LEVEL FLUCTUATING ( 5 FDA reports)
DRUG PRESCRIBING ERROR ( 5 FDA reports)
DYSTONIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 5 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
EOSINOPHILIA ( 5 FDA reports)
EXCORIATION ( 5 FDA reports)
EXOSTOSIS ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEMIPLEGIA ( 5 FDA reports)
HEPATIC ENCEPHALOPATHY ( 5 FDA reports)
HEPATITIS A ( 5 FDA reports)
HEPATITIS CHOLESTATIC ( 5 FDA reports)
HEPATORENAL SYNDROME ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HYPERAESTHESIA ( 5 FDA reports)
HYPERLIPIDAEMIA ( 5 FDA reports)
HYPERTONIC BLADDER ( 5 FDA reports)
IMMOBILE ( 5 FDA reports)
IMPRISONMENT ( 5 FDA reports)
INCREASED APPETITE ( 5 FDA reports)
INITIAL INSOMNIA ( 5 FDA reports)
ISCHAEMIC STROKE ( 5 FDA reports)
JOINT CREPITATION ( 5 FDA reports)
JOINT INJURY ( 5 FDA reports)
JOINT STIFFNESS ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 5 FDA reports)
LUNG INFECTION ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
MASS ( 5 FDA reports)
MENIERE'S DISEASE ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
MOUTH ULCERATION ( 5 FDA reports)
MUSCULOSKELETAL DISORDER ( 5 FDA reports)
NEURITIS ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 5 FDA reports)
OCULAR HYPERAEMIA ( 5 FDA reports)
OESOPHAGEAL DISORDER ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PARTIAL SEIZURES ( 5 FDA reports)
PITTING OEDEMA ( 5 FDA reports)
POST PROCEDURAL PAIN ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PURPURA ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 5 FDA reports)
RENAL ARTERY OCCLUSION ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RENAL TRANSPLANT ( 5 FDA reports)
RENAL TUBULAR NECROSIS ( 5 FDA reports)
RETINAL DISORDER ( 5 FDA reports)
RHINITIS ( 5 FDA reports)
SCRATCH ( 5 FDA reports)
SICK SINUS SYNDROME ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SKIN IRRITATION ( 5 FDA reports)
SLUGGISHNESS ( 5 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
TOOTH ABSCESS ( 5 FDA reports)
TOOTH DISCOLOURATION ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 4 FDA reports)
ABORTION SPONTANEOUS ( 4 FDA reports)
ACCIDENT AT WORK ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 4 FDA reports)
AKATHISIA ( 4 FDA reports)
ALDOLASE INCREASED ( 4 FDA reports)
AMMONIA INCREASED ( 4 FDA reports)
ANEURYSM ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 4 FDA reports)
APHONIA ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
ARTERIAL DISORDER ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ATRIAL FLUTTER ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLOOD BICARBONATE DECREASED ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD MAGNESIUM INCREASED ( 4 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CARDIAC FLUTTER ( 4 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 4 FDA reports)
CATARACT OPERATION ( 4 FDA reports)
CEREBRAL ISCHAEMIA ( 4 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 4 FDA reports)
CHRONIC SINUSITIS ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
COLITIS ISCHAEMIC ( 4 FDA reports)
COLON CANCER ( 4 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 4 FDA reports)
CREPITATIONS ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CYST ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DEVICE FAILURE ( 4 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 4 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 4 FDA reports)
ENURESIS ( 4 FDA reports)
FACIAL PARESIS ( 4 FDA reports)
FAECES DISCOLOURED ( 4 FDA reports)
FOOD AVERSION ( 4 FDA reports)
FOOD CRAVING ( 4 FDA reports)
FURUNCLE ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERVENTILATION ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOTONIA ( 4 FDA reports)
HYPOVOLAEMIC SHOCK ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
IMMUNE SYSTEM DISORDER ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 4 FDA reports)
INJECTION SITE REACTION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 4 FDA reports)
IRRITABLE BOWEL SYNDROME ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
LACERATION ( 4 FDA reports)
LACRIMAL DISORDER ( 4 FDA reports)
LIVER TRANSPLANT ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOSS OF EMPLOYMENT ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
LYMPHOEDEMA ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
METABOLIC DISORDER ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
METASTASES TO LYMPH NODES ( 4 FDA reports)
MUSCLE STRAIN ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NERVE COMPRESSION ( 4 FDA reports)
NEUROMA ( 4 FDA reports)
NEUROPATHIC PAIN ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 4 FDA reports)
NOSOCOMIAL INFECTION ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
OVERWEIGHT ( 4 FDA reports)
PANIC REACTION ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POOR PERIPHERAL CIRCULATION ( 4 FDA reports)
POST PROCEDURAL VOMITING ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROTEIN TOTAL DECREASED ( 4 FDA reports)
PRURITUS GENERALISED ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RETINAL DETACHMENT ( 4 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 4 FDA reports)
SNEEZING ( 4 FDA reports)
SPINAL CORD COMPRESSION ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
SPONDYLITIS ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
TENSION ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
TOE AMPUTATION ( 4 FDA reports)
TONGUE DISORDER ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VARICOSE VEIN ( 4 FDA reports)
VASCULAR OCCLUSION ( 4 FDA reports)
VASCULITIS ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
WEIGHT LOSS POOR ( 4 FDA reports)
WRIST FRACTURE ( 4 FDA reports)
ABDOMINAL INJURY ( 3 FDA reports)
ABDOMINAL RIGIDITY ( 3 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
AMENORRHOEA ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
ANTICONVULSANT TOXICITY ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 3 FDA reports)
AORTIC OCCLUSION ( 3 FDA reports)
APATHY ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
APHTHOUS STOMATITIS ( 3 FDA reports)
APNOEA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
BLADDER OPERATION ( 3 FDA reports)
BLADDER SPASM ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CREATINE INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRUXISM ( 3 FDA reports)
CARDIAC ANEURYSM ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CAROTID ARTERY DISEASE ( 3 FDA reports)
CAROTID ARTERY OCCLUSION ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHEST WALL PAIN ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTECTOMY ( 3 FDA reports)
CHROMATOPSIA ( 3 FDA reports)
COELIAC DISEASE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
CORNEAL INFECTION ( 3 FDA reports)
CRACKLES LUNG ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYANOPSIA ( 3 FDA reports)
CYTOLYTIC HEPATITIS ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DEATH OF RELATIVE ( 3 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 3 FDA reports)
DIABETIC COMPLICATION ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DIVERTICULAR PERFORATION ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG RESISTANCE ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPHASIA ( 3 FDA reports)
EAR CONGESTION ( 3 FDA reports)
EAR DISCOMFORT ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE OPERATION ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
FEBRILE NEUTROPENIA ( 3 FDA reports)
FEELING OF DESPAIR ( 3 FDA reports)
FLAT AFFECT ( 3 FDA reports)
FLUID OVERLOAD ( 3 FDA reports)
FOOD ALLERGY ( 3 FDA reports)
FOOD POISONING ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC STROKE ( 3 FDA reports)
HAND FRACTURE ( 3 FDA reports)
HEAD DISCOMFORT ( 3 FDA reports)
HEART RATE ABNORMAL ( 3 FDA reports)
HEAT EXHAUSTION ( 3 FDA reports)
HELICOBACTER INFECTION ( 3 FDA reports)
HEPATIC CYST ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HOARSENESS ( 3 FDA reports)
HOMICIDAL IDEATION ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERPHAGIA ( 3 FDA reports)
HYPERURICAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
HYPOTRICHOSIS ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INCREASED TENDENCY TO BRUISE ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INJECTION SITE BRUISING ( 3 FDA reports)
INJURY ASPHYXIATION ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LEG AMPUTATION ( 3 FDA reports)
LEUKOPENIA ( 3 FDA reports)
LIGAMENT INJURY ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LIP ULCERATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MASTICATION DISORDER ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENISCUS LESION ( 3 FDA reports)
MENORRHAGIA ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MIOSIS ( 3 FDA reports)
MONOPLEGIA ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCLE FATIGUE ( 3 FDA reports)
MUSCLE RUPTURE ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEOPLASM ( 3 FDA reports)
NEOPLASM RECURRENCE ( 3 FDA reports)
NEUROLOGICAL SYMPTOM ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 3 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 3 FDA reports)
OPTIC NERVE INJURY ( 3 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 3 FDA reports)
ORGASM ABNORMAL ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PANCREATIC DISORDER ( 3 FDA reports)
PANIC DISORDER ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PAROTID GLAND ENLARGEMENT ( 3 FDA reports)
PCO2 DECREASED ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PH URINE DECREASED ( 3 FDA reports)
PHARYNGEAL ERYTHEMA ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYMYALGIA ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POST POLIO SYNDROME ( 3 FDA reports)
POSTOPERATIVE INFECTION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROTEIN URINE ( 3 FDA reports)
PSYCHOSOMATIC DISEASE ( 3 FDA reports)
PULMONARY THROMBOSIS ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
RADIATION INJURY ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECURRENT CANCER ( 3 FDA reports)
RENAL CORTICAL NECROSIS ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RETINAL TEAR ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SCHIZOPHRENIA ( 3 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SINUS PAIN ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPINAL DEFORMITY ( 3 FDA reports)
SPINAL FUSION SURGERY ( 3 FDA reports)
SPLEEN CONGESTION ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STENT OCCLUSION ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SUDDEN HEARING LOSS ( 3 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THIRST ( 3 FDA reports)
THYROXINE DECREASED ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TOOTH DECALCIFICATION ( 3 FDA reports)
TRICUSPID VALVE DISEASE ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
TUNNEL VISION ( 3 FDA reports)
UPPER LIMB FRACTURE ( 3 FDA reports)
URINE FLOW DECREASED ( 3 FDA reports)
VAGINAL DISORDER ( 3 FDA reports)
VAGINAL INFECTION ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
VESTIBULAR DISORDER ( 3 FDA reports)
VITH NERVE PARALYSIS ( 3 FDA reports)
WOUND ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALCOHOLIC LIVER DISEASE ( 2 FDA reports)
ALLERGY TO ANIMAL ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
ARTERIAL BYPASS OPERATION ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ARTHROPOD STING ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATROPHY ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
AUTOIMMUNE HEPATITIS ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 2 FDA reports)
BITE ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLADDER NEOPLASM ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLADDER PROLAPSE ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLINDNESS CORTICAL ( 2 FDA reports)
BLOOD BICARBONATE INCREASED ( 2 FDA reports)
BLOOD CAFFEINE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 2 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN NEOPLASM BENIGN ( 2 FDA reports)
BRAIN OPERATION ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
BRONCHITIS CHRONIC ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CAFFEINE CONSUMPTION ( 2 FDA reports)
CANDIDURIA ( 2 FDA reports)
CARDIAC FIBRILLATION ( 2 FDA reports)
CARDIAC OUTPUT DECREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOVERSION ( 2 FDA reports)
CAROTID ARTERY ATHEROMA ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL SARCOIDOSIS ( 2 FDA reports)
CERVICOGENIC HEADACHE ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLECYSTITIS INFECTIVE ( 2 FDA reports)
CHONDROLYSIS ( 2 FDA reports)
CHRONIC FATIGUE SYNDROME ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLUMSINESS ( 2 FDA reports)
COLITIS COLLAGENOUS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
COLOSTOMY ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONFABULATION ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CONVULSION NEONATAL ( 2 FDA reports)
COR PULMONALE ( 2 FDA reports)
CORNEAL OPACITY ( 2 FDA reports)
DEATH OF PARENT ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DECREASED INTEREST ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DENGUE FEVER ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATOMYOSITIS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG CLEARANCE DECREASED ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DYSENTERY ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSPHORIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROCONVULSIVE THERAPY ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
EPIDERMAL NECROSIS ( 2 FDA reports)
EROSIVE OESOPHAGITIS ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
EXERCISE LACK OF ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYELID DISORDER ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FEAR OF FALLING ( 2 FDA reports)
FEELING HOT AND COLD ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOETAL HEART RATE DECREASED ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GAMBLING ( 2 FDA reports)
GASTRIC BYPASS ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL CARCINOMA ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLIOBLASTOMA ( 2 FDA reports)
GOITRE ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
GYNAECOMASTIA ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAIR TEXTURE ABNORMAL ( 2 FDA reports)
HALLUCINATION, TACTILE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATITIS C VIRUS ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HERPES VIRUS INFECTION ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HILAR LYMPHADENOPATHY ( 2 FDA reports)
HIP SURGERY ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HOSPITALISATION ( 2 FDA reports)
HUMERUS FRACTURE ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
HYSTERECTOMY ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 2 FDA reports)
INCISION SITE COMPLICATION ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
INJECTION SITE CALCIFICATION ( 2 FDA reports)
INJECTION SITE DISCHARGE ( 2 FDA reports)
INJECTION SITE INFECTION ( 2 FDA reports)
INNER EAR DISORDER ( 2 FDA reports)
INSULIN RESISTANCE ( 2 FDA reports)
INSULIN-REQUIRING TYPE II DIABETES MELLITUS ( 2 FDA reports)
INTERMITTENT CLAUDICATION ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTRAOCULAR PRESSURE TEST ABNORMAL ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IVTH NERVE PARALYSIS ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 2 FDA reports)
KIDNEY SMALL ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LIMB TRAUMATIC AMPUTATION ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP DRY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LIPIDS INCREASED ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCKED-IN SYNDROME ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
LOSS OF LIBIDO ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN ABNORMAL ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MALIGNANT NEOPLASM OF EYE ( 2 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MICTURITION FREQUENCY DECREASED ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MITRAL VALVE REPLACEMENT ( 2 FDA reports)
MOLE EXCISION ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCLE SWELLING ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MYOPATHY STEROID ( 2 FDA reports)
MYOPIA ( 2 FDA reports)
NARCOLEPSY ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL POLYPS ( 2 FDA reports)
NASAL SINUS DRAINAGE ( 2 FDA reports)
NASAL TURBINATE HYPERTROPHY ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUROFIBROMATOSIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NO ADVERSE DRUG EFFECT ( 2 FDA reports)
NODAL RHYTHM ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OBSTRUCTION ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OCULAR HYPERTENSION ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 2 FDA reports)
ONYCHOMYCOSIS ( 2 FDA reports)
OOPHORECTOMY ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL MUCOSA EROSION ( 2 FDA reports)
ORAL MUCOSAL BLISTERING ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
OVARIAN ENLARGEMENT ( 2 FDA reports)
PACEMAKER COMPLICATION ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PARAPLEGIA ( 2 FDA reports)
PATHOGEN RESISTANCE ( 2 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERIORBITAL HAEMATOMA ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 2 FDA reports)
PERIPHERAL NERVE PALSY ( 2 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 2 FDA reports)
PHOTOKERATITIS ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
PHYSICAL ASSAULT ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PIRIFORMIS SYNDROME ( 2 FDA reports)
POLYCYTHAEMIA VERA ( 2 FDA reports)
POLYMYALGIA RHEUMATICA ( 2 FDA reports)
POLYP ( 2 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 2 FDA reports)
PRIAPISM ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROSTATIC OPERATION ( 2 FDA reports)
PSORIATIC ARTHROPATHY ( 2 FDA reports)
PSYCHOGENIC PAIN DISORDER ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY MASS ( 2 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
PYURIA ( 2 FDA reports)
QUADRIPARESIS ( 2 FDA reports)
REACTION TO PRESERVATIVES ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
REFLEX SYMPATHETIC DYSTROPHY ( 2 FDA reports)
REFLUX OESOPHAGITIS ( 2 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 2 FDA reports)
RETINAL VASCULAR DISORDER ( 2 FDA reports)
RETINOPATHY HYPERTENSIVE ( 2 FDA reports)
RHINOVIRUS INFECTION ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SARCOIDOSIS ( 2 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 2 FDA reports)
SCOLIOSIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SHOULDER ARTHROPLASTY ( 2 FDA reports)
SIDEROBLASTIC ANAEMIA ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUS OPERATION ( 2 FDA reports)
SINUS POLYP ( 2 FDA reports)
SKIN REACTION ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 2 FDA reports)
SOFT TISSUE DISORDER ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPINAL CORD INJURY ( 2 FDA reports)
SPLENECTOMY ( 2 FDA reports)
SPUTUM DISCOLOURED ( 2 FDA reports)
STARING ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
THERAPEUTIC PROCEDURE ( 2 FDA reports)
THERAPY REGIMEN CHANGED ( 2 FDA reports)
THROAT CANCER ( 2 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
THYROID NEOPLASM ( 2 FDA reports)
TOE DEFORMITY ( 2 FDA reports)
TONGUE BLACK HAIRY ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRIGEMINAL NEURALGIA ( 2 FDA reports)
TRISMUS ( 2 FDA reports)
ULNAR NERVE INJURY ( 2 FDA reports)
UMBILICAL HERNIA ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
URINE COLOUR ABNORMAL ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL DISCHARGE ( 2 FDA reports)
VASOCONSTRICTION ( 2 FDA reports)
VEIN DISCOLOURATION ( 2 FDA reports)
VENOUS INJURY ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 2 FDA reports)
VICTIM OF CHILD ABUSE ( 2 FDA reports)
VICTIM OF CRIME ( 2 FDA reports)
VITAMIN B12 INCREASED ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
VITREOUS DISORDER ( 2 FDA reports)
VULVOVAGINAL DISCOMFORT ( 2 FDA reports)
WATER POLLUTION ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
XANTHOPSIA ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL OPERATION ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABORTION INCOMPLETE ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENOCORTICAL CARCINOMA ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALOPECIA EFFLUVIUM ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANASTOMOTIC LEAK ( 1 FDA reports)
ANGIOGRAM ABNORMAL ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
APPLICATION SITE DISCOLOURATION ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL STENOSIS ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIAL STENT INSERTION ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTERITIS ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASTHMATIC CRISIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
AUDIOGRAM ABNORMAL ( 1 FDA reports)
AUTOIMMUNE THYROIDITIS ( 1 FDA reports)
AUTOTRANSFUSION ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA URINE NO ORGANISM OBSERVED ( 1 FDA reports)
BACTERIAL CULTURE POSITIVE ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE ABNORMAL ( 1 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 1 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 1 FDA reports)
BIOPSY MUSCLE ( 1 FDA reports)
BLADDER CATHETER REPLACEMENT ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ETHANOL ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO DECREASED ( 1 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BODY TEMPERATURE FLUCTUATION ( 1 FDA reports)
BONE FISSURE ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 1 FDA reports)
BRADYKINESIA ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER RECURRENT ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BUNION ( 1 FDA reports)
BURGLARY VICTIM ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URINARY ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC NEOPLASM MALIGNANT ( 1 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 1 FDA reports)
CARDIAC PERFORATION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARTILAGE GRAFT ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CARTILAGE NEOPLASM ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL PALSY ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBROSPINAL FLUID LEAKAGE ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CERVICAL MYELOPATHY ( 1 FDA reports)
CERVICAL SPINAL STENOSIS ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEMICAL ABUSER ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLUSTER HEADACHE ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
COLON INJURY ( 1 FDA reports)
COLONIC HAEMORRHAGE ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CONFUSION POSTOPERATIVE ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
COPROLALIA ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COSTOCHONDRITIS ( 1 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CSF CELL COUNT ABNORMAL ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTOPEXY ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DEAFNESS BILATERAL ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
DELUSION OF GRANDEUR ( 1 FDA reports)
DENTAL NECROSIS ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DIABETIC COMA ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISLOCATION OF VERTEBRA ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DISTURBANCE IN SEXUAL AROUSAL ( 1 FDA reports)
DRUG CHEMICAL INCOMPATIBILITY ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG TOLERANCE DECREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSACUSIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSLOGIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPRAXIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSTROPHIA MYOTONICA ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR NEOPLASM MALIGNANT ( 1 FDA reports)
EJACULATION FAILURE ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROPHORESIS PROTEIN ABNORMAL ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY UPPER GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NAEVUS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
ERYTHROPSIA ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUSTACHIAN TUBE DISORDER ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXSANGUINATION ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE OEDEMA ( 1 FDA reports)
EYE OPERATION COMPLICATION ( 1 FDA reports)
EYE REDNESS ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FAILURE TO ANASTOMOSE ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT TISSUE INCREASED ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING GUILTY ( 1 FDA reports)
FEELING OF RELAXATION ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUNGAEMIA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENITAL INFECTION BACTERIAL ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL ATROPHY ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GINGIVAL HYPERPLASIA ( 1 FDA reports)
GINGIVAL HYPERTROPHY ( 1 FDA reports)
GINGIVAL OEDEMA ( 1 FDA reports)
GINGIVAL OPERATION ( 1 FDA reports)
GINGIVAL RECESSION ( 1 FDA reports)
GINGIVAL ULCERATION ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS INCREASED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
GRAFT COMPLICATION ( 1 FDA reports)
GRAFT INFECTION ( 1 FDA reports)
GRANULOCYTE COUNT INCREASED ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMOGLOBIN URINE PRESENT ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HAPTOGLOBIN INCREASED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEAT RASH ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS A VIRUS ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERDYNAMIC PRECORDIUM ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPERTROPHY BREAST ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGEUSIA ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IATROGENIC INFECTION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INADEQUATE DIET ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE ULCER ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL PROLAPSE ( 1 FDA reports)
INTESTINAL RESECTION ( 1 FDA reports)
INTESTINAL SPASM ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON METABOLISM DISORDER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT LIGAMENT RUPTURE ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACRIMATION DECREASED ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL DISORDER ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LARYNX IRRITATION ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEUKAEMIA ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIBIDO INCREASED ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP EROSION ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOOSE BODY IN JOINT ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LOOSE TOOTH ( 1 FDA reports)
LOSS OF PROPRIOCEPTION ( 1 FDA reports)
LOWER LIMB DEFORMITY ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE III ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG OPERATION ( 1 FDA reports)
LUPUS NEPHRITIS ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECONIUM ABNORMAL ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO KIDNEY ( 1 FDA reports)
METASTASES TO SPLEEN ( 1 FDA reports)
METASTASES TO THE RESPIRATORY SYSTEM ( 1 FDA reports)
METASTATIC GASTRIC CANCER ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICROSURGERY TO HAND ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MIGRATION OF IMPLANT ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MORBID THOUGHTS ( 1 FDA reports)
MOTION SICKNESS ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE NECROSIS ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYCOTIC CORNEAL ULCER ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL ODOUR ( 1 FDA reports)
NECK MASS ( 1 FDA reports)
NEONATAL ANOXIA ( 1 FDA reports)
NEONATAL HYPOXIA ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEPHROSCLEROSIS ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEURODERMATITIS ( 1 FDA reports)
NEURODEVELOPMENTAL DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NICOTINE DEPENDENCE ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGEAL FISTULA ( 1 FDA reports)
OESOPHAGEAL OPERATION ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPISTHOTONUS ( 1 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEITIS DEFORMANS ( 1 FDA reports)
OSTEOCHONDROSIS ( 1 FDA reports)
OSTEOGENESIS IMPERFECTA ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAINFUL DEFAECATION ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAESTHESIA OF GENITAL MALE ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PAROXYSMAL PERCEPTUAL ALTERATION ( 1 FDA reports)
PATELLA FRACTURE ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE ABNORMAL ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PELVIC VENOUS THROMBOSIS ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE BLISTER ( 1 FDA reports)
PENILE HAEMORRHAGE ( 1 FDA reports)
PENILE SIZE REDUCED ( 1 FDA reports)
PEPTIC ULCER PERFORATION ( 1 FDA reports)
PERINEAL ABSCESS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIRENAL HAEMATOMA ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHANTOM PAIN ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PITUITARY TUMOUR ( 1 FDA reports)
PLASMA VISCOSITY DECREASED ( 1 FDA reports)
PLATELET AGGREGATION ABNORMAL ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
POLIOMYELITIS ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POLYDACTYLY ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYSUBSTANCE ABUSE ( 1 FDA reports)
POOR SUCKING REFLEX ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PORTAL VEIN OCCLUSION ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST HERPETIC NEURALGIA ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL DIZZINESS ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
POSTMENOPAUSE ( 1 FDA reports)
POSTNASAL DRIP ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
PRECANCEROUS CELLS PRESENT ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROSTATECTOMY ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PSEUDO-BARTTER SYNDROME ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELECTASIA ( 1 FDA reports)
PYLORIC STENOSIS ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
RADICAL PROSTATECTOMY ( 1 FDA reports)
RADICULITIS ( 1 FDA reports)
RADIOTHERAPY TO PROSTATE ( 1 FDA reports)
RALES ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULOSQUAMOUS ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL NEOPLASM ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RECTAL TENESMUS ( 1 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL MASS ( 1 FDA reports)
RENAL STONE REMOVAL ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL ARTERY OCCLUSION ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL NEOVASCULARISATION ( 1 FDA reports)
RHEUMATOID FACTOR INCREASED ( 1 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
ROSAI-DORFMAN SYNDROME ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERODERMA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SERUM SEROTONIN DECREASED ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN NEOPLASM EXCISION ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMOKER ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
SOMATIC DELUSION ( 1 FDA reports)
SPASTIC PARAPLEGIA ( 1 FDA reports)
SPIDER NAEVUS ( 1 FDA reports)
SPINAL CORD NEOPLASM ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
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SPINAL CORD PARALYSIS ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPINAL LIGAMENT OSSIFICATION ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPONTANEOUS PENILE ERECTION ( 1 FDA reports)
SPORTS INJURY ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STASIS DERMATITIS ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOOL ANALYSIS ABNORMAL ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
SUBDURAL EFFUSION ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUFFOCATION FEELING ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPORAL ARTERITIS ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
TESTICULAR PAIN ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
TETANUS ( 1 FDA reports)
TETANY ( 1 FDA reports)
THALAMUS HAEMORRHAGE ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
THORACIC OUTLET SYNDROME ( 1 FDA reports)
THROAT LESION ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID FUNCTION TEST NORMAL ( 1 FDA reports)
THYROID GLAND CANCER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
THYROIDITIS ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TIBIA FRACTURE ( 1 FDA reports)
TIC ( 1 FDA reports)
TOBACCO ABUSE ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH HYPOPLASIA ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOTAL CHOLESTEROL/HDL RATIO INCREASED ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRANCE ( 1 FDA reports)
TRANSFUSION REACTION ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
UNDERWEIGHT ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL OBSTRUCTION ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT OPERATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
UROBILIN URINE PRESENT ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
UTERINE DILATION AND CURETTAGE ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VAGAL NERVE STIMULATOR IMPLANTATION ( 1 FDA reports)
VAGINAL CYST ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VAGUS NERVE DISORDER ( 1 FDA reports)
VASCULAR ENCEPHALOPATHY ( 1 FDA reports)
VASCULAR RUPTURE ( 1 FDA reports)
VASECTOMY ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR FLUTTER ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL COLUMN MASS ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VIRAL PERICARDITIS ( 1 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOCAL CORD POLYP ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL DISORDER ( 1 FDA reports)
WEIGHT ABNORMAL ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)
X-RAY LIMB ABNORMAL ( 1 FDA reports)

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