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

PSYCHOTIC DISORDER ( 307 FDA reports)
DRUG INTERACTION ( 276 FDA reports)
SCHIZOPHRENIA ( 218 FDA reports)
WEIGHT INCREASED ( 178 FDA reports)
DIABETES MELLITUS ( 161 FDA reports)
PYREXIA ( 144 FDA reports)
ANXIETY ( 140 FDA reports)
MALAISE ( 138 FDA reports)
HALLUCINATION, AUDITORY ( 136 FDA reports)
COMPLETED SUICIDE ( 131 FDA reports)
HYPERTENSION ( 123 FDA reports)
NEUTROPENIA ( 120 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 119 FDA reports)
AGITATION ( 117 FDA reports)
DEPRESSION ( 112 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 111 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 109 FDA reports)
CONVULSION ( 102 FDA reports)
SEDATION ( 101 FDA reports)
SUICIDAL IDEATION ( 101 FDA reports)
DRUG INEFFECTIVE ( 99 FDA reports)
URINARY TRACT INFECTION ( 98 FDA reports)
CONDITION AGGRAVATED ( 96 FDA reports)
SOMNOLENCE ( 95 FDA reports)
AGGRESSION ( 93 FDA reports)
DEATH ( 93 FDA reports)
DIZZINESS ( 93 FDA reports)
FATIGUE ( 93 FDA reports)
DELUSION ( 92 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 92 FDA reports)
TACHYCARDIA ( 91 FDA reports)
NEUTROPHIL COUNT DECREASED ( 89 FDA reports)
OVERDOSE ( 89 FDA reports)
VOMITING ( 89 FDA reports)
SUICIDE ATTEMPT ( 88 FDA reports)
HAEMOGLOBIN DECREASED ( 87 FDA reports)
NEUTROPHIL COUNT INCREASED ( 87 FDA reports)
WEIGHT DECREASED ( 86 FDA reports)
FALL ( 85 FDA reports)
SINUS TACHYCARDIA ( 84 FDA reports)
DYSPNOEA ( 83 FDA reports)
LEUKOPENIA ( 83 FDA reports)
TREMOR ( 82 FDA reports)
INSOMNIA ( 81 FDA reports)
CONFUSIONAL STATE ( 80 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 80 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 79 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 78 FDA reports)
ABNORMAL BEHAVIOUR ( 76 FDA reports)
DIARRHOEA ( 75 FDA reports)
HEART RATE INCREASED ( 75 FDA reports)
CONSTIPATION ( 74 FDA reports)
NAUSEA ( 74 FDA reports)
MENTAL IMPAIRMENT ( 73 FDA reports)
TREATMENT NONCOMPLIANCE ( 70 FDA reports)
SALIVARY HYPERSECRETION ( 68 FDA reports)
URINARY INCONTINENCE ( 67 FDA reports)
CHEST PAIN ( 66 FDA reports)
AKATHISIA ( 61 FDA reports)
DYSPHAGIA ( 61 FDA reports)
HALLUCINATION ( 60 FDA reports)
RHABDOMYOLYSIS ( 60 FDA reports)
RENAL FAILURE ACUTE ( 57 FDA reports)
PLATELET COUNT DECREASED ( 56 FDA reports)
ASTHENIA ( 55 FDA reports)
CATATONIA ( 54 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 52 FDA reports)
DYSTONIA ( 52 FDA reports)
HEADACHE ( 52 FDA reports)
MENTAL DISORDER ( 52 FDA reports)
PNEUMONIA ( 52 FDA reports)
HYPOGLYCAEMIA ( 51 FDA reports)
MANIA ( 51 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 50 FDA reports)
TYPE 2 DIABETES MELLITUS ( 50 FDA reports)
BLOOD PROLACTIN INCREASED ( 49 FDA reports)
GAIT DISTURBANCE ( 49 FDA reports)
HYPERGLYCAEMIA ( 49 FDA reports)
HYPERPROLACTINAEMIA ( 49 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 49 FDA reports)
PARANOIA ( 49 FDA reports)
IRRITABILITY ( 48 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 47 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 47 FDA reports)
CARDIAC ARREST ( 46 FDA reports)
TARDIVE DYSKINESIA ( 46 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 46 FDA reports)
DEPRESSED MOOD ( 45 FDA reports)
OBESITY ( 44 FDA reports)
SKIN DISORDER ( 44 FDA reports)
VISION BLURRED ( 44 FDA reports)
HIATUS HERNIA ( 43 FDA reports)
PANCREATITIS ( 43 FDA reports)
PREMATURE BABY ( 42 FDA reports)
RASH ( 42 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 41 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 41 FDA reports)
HYPERHIDROSIS ( 41 FDA reports)
ABDOMINAL PAIN ( 40 FDA reports)
PAIN ( 40 FDA reports)
PHYSICAL ASSAULT ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 39 FDA reports)
PULMONARY EMBOLISM ( 39 FDA reports)
BACK PAIN ( 38 FDA reports)
CARDIAC MURMUR ( 38 FDA reports)
GRANULOCYTOPENIA ( 38 FDA reports)
HYPOTENSION ( 38 FDA reports)
MUSCULAR WEAKNESS ( 38 FDA reports)
PREMATURE LABOUR ( 38 FDA reports)
ABDOMINAL TENDERNESS ( 37 FDA reports)
DYSARTHRIA ( 37 FDA reports)
HOMICIDAL IDEATION ( 37 FDA reports)
LETHARGY ( 37 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 37 FDA reports)
STAPHYLOCOCCAL INFECTION ( 37 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 36 FDA reports)
CEREBROVASCULAR ACCIDENT ( 36 FDA reports)
CHOLESTASIS OF PREGNANCY ( 36 FDA reports)
LIVE BIRTH ( 36 FDA reports)
PARKINSONISM ( 36 FDA reports)
ANAEMIA ( 35 FDA reports)
ATRIAL SEPTAL DEFECT ( 35 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 34 FDA reports)
BLOOD PRESSURE INCREASED ( 34 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 34 FDA reports)
MONOCYTE COUNT INCREASED ( 34 FDA reports)
RESPIRATORY ARREST ( 34 FDA reports)
BODY MASS INDEX DECREASED ( 33 FDA reports)
IRON DEFICIENCY ANAEMIA ( 33 FDA reports)
MEAN CELL VOLUME DECREASED ( 33 FDA reports)
SEPSIS ( 33 FDA reports)
THROMBOCYTOPENIA ( 33 FDA reports)
DRUG LEVEL INCREASED ( 32 FDA reports)
HYPERLIPIDAEMIA ( 32 FDA reports)
PAIN IN EXTREMITY ( 32 FDA reports)
THROMBOCYTOSIS ( 32 FDA reports)
DIABETIC KETOACIDOSIS ( 31 FDA reports)
DYSKINESIA ( 31 FDA reports)
GALACTORRHOEA ( 31 FDA reports)
MYOCARDIAL INFARCTION ( 31 FDA reports)
URINARY RETENTION ( 31 FDA reports)
METABOLIC DISORDER ( 30 FDA reports)
OESOPHAGITIS ( 30 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 29 FDA reports)
DECREASED APPETITE ( 29 FDA reports)
DISORIENTATION ( 29 FDA reports)
HYPOKALAEMIA ( 29 FDA reports)
OEDEMA PERIPHERAL ( 29 FDA reports)
RESTLESSNESS ( 29 FDA reports)
SEROTONIN SYNDROME ( 29 FDA reports)
DRUG TOXICITY ( 28 FDA reports)
HAEMATOCRIT DECREASED ( 28 FDA reports)
HEPATIC STEATOSIS ( 28 FDA reports)
SYNCOPE ( 28 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 27 FDA reports)
DISTURBANCE IN ATTENTION ( 27 FDA reports)
HYPOMANIA ( 27 FDA reports)
INTENTIONAL OVERDOSE ( 27 FDA reports)
PLATELET COUNT INCREASED ( 27 FDA reports)
PSYCHIATRIC SYMPTOM ( 27 FDA reports)
RENAL IMPAIRMENT ( 27 FDA reports)
BODY TEMPERATURE INCREASED ( 26 FDA reports)
GASTRITIS ( 26 FDA reports)
HYPOAESTHESIA ( 26 FDA reports)
PANCREATITIS ACUTE ( 26 FDA reports)
BLOOD GLUCOSE INCREASED ( 25 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 25 FDA reports)
EOSINOPHILIA ( 25 FDA reports)
PULMONARY CONGESTION ( 25 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 25 FDA reports)
RENAL FAILURE ( 25 FDA reports)
RESTLESS LEGS SYNDROME ( 25 FDA reports)
SUDDEN DEATH ( 25 FDA reports)
ASTHMA ( 24 FDA reports)
CHOLINERGIC SYNDROME ( 24 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 24 FDA reports)
LYMPHADENOPATHY ( 24 FDA reports)
PREGNANCY ( 24 FDA reports)
RESPIRATORY FAILURE ( 24 FDA reports)
WHITE BLOOD CELL DISORDER ( 24 FDA reports)
CHEST DISCOMFORT ( 23 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 23 FDA reports)
HEPATIC FAILURE ( 23 FDA reports)
MOOD ALTERED ( 23 FDA reports)
MYOCARDITIS ( 23 FDA reports)
MYOCLONUS ( 23 FDA reports)
PNEUMOTHORAX ( 23 FDA reports)
POLYDIPSIA ( 23 FDA reports)
RASH ERYTHEMATOUS ( 23 FDA reports)
SEXUAL DYSFUNCTION ( 23 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 22 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 22 FDA reports)
BIPOLAR DISORDER ( 22 FDA reports)
HYPOPHAGIA ( 22 FDA reports)
LACTIC ACIDOSIS ( 22 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 22 FDA reports)
METABOLIC SYNDROME ( 22 FDA reports)
STRESS ( 22 FDA reports)
ANTISOCIAL BEHAVIOUR ( 21 FDA reports)
CARDIAC DISORDER ( 21 FDA reports)
CIRCULATORY COLLAPSE ( 21 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 21 FDA reports)
COUGH ( 21 FDA reports)
INFECTION ( 21 FDA reports)
MENORRHAGIA ( 21 FDA reports)
PULMONARY FIBROSIS ( 21 FDA reports)
ABDOMINAL PAIN UPPER ( 20 FDA reports)
AFFECT LABILITY ( 20 FDA reports)
ATAXIA ( 20 FDA reports)
BIPOLAR I DISORDER ( 20 FDA reports)
BRADYCARDIA ( 20 FDA reports)
CARDIAC FAILURE ( 20 FDA reports)
CELLULITIS ( 20 FDA reports)
DISINHIBITION ( 20 FDA reports)
FEELING ABNORMAL ( 20 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 20 FDA reports)
INTENTIONAL DRUG MISUSE ( 20 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 20 FDA reports)
MENTAL STATUS CHANGES ( 20 FDA reports)
OROPHARYNGEAL PAIN ( 20 FDA reports)
SPEECH DISORDER ( 20 FDA reports)
THINKING ABNORMAL ( 20 FDA reports)
ANGER ( 19 FDA reports)
COORDINATION ABNORMAL ( 19 FDA reports)
DELIRIUM ( 19 FDA reports)
DRY MOUTH ( 19 FDA reports)
LOSS OF CONSCIOUSNESS ( 19 FDA reports)
MUSCLE RIGIDITY ( 19 FDA reports)
MYELODYSPLASTIC SYNDROME ( 19 FDA reports)
PALPITATIONS ( 19 FDA reports)
PERSECUTORY DELUSION ( 19 FDA reports)
PLEURAL EFFUSION ( 19 FDA reports)
PSYCHOMOTOR RETARDATION ( 19 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 19 FDA reports)
SNORING ( 19 FDA reports)
TIC ( 19 FDA reports)
WHEEZING ( 19 FDA reports)
APPENDICITIS ( 18 FDA reports)
BRADYKINESIA ( 18 FDA reports)
DIABETIC COMA ( 18 FDA reports)
GRAND MAL CONVULSION ( 18 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 18 FDA reports)
NERVOUSNESS ( 18 FDA reports)
SUSPICIOUSNESS ( 18 FDA reports)
ARRHYTHMIA ( 17 FDA reports)
ASPIRATION ( 17 FDA reports)
BALANCE DISORDER ( 17 FDA reports)
BLOOD CREATININE INCREASED ( 17 FDA reports)
BLOOD PRESSURE DECREASED ( 17 FDA reports)
DYSPHONIA ( 17 FDA reports)
EMOTIONAL DISTRESS ( 17 FDA reports)
ENCEPHALOPATHY ( 17 FDA reports)
EOSINOPHIL COUNT INCREASED ( 17 FDA reports)
HEPATITIS C ( 17 FDA reports)
HYPOTHYROIDISM ( 17 FDA reports)
METASTASES TO BONE ( 17 FDA reports)
OSTEOMYELITIS ( 17 FDA reports)
PNEUMONIA ASPIRATION ( 17 FDA reports)
SLEEP DISORDER ( 17 FDA reports)
UNRESPONSIVE TO STIMULI ( 17 FDA reports)
APATHY ( 16 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 16 FDA reports)
BLOOD SODIUM DECREASED ( 16 FDA reports)
DEEP VEIN THROMBOSIS ( 16 FDA reports)
FEAR ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
INTENTIONAL SELF-INJURY ( 16 FDA reports)
PANIC ATTACK ( 16 FDA reports)
PARAESTHESIA ( 16 FDA reports)
POISONING ( 16 FDA reports)
POLYP ( 16 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 16 FDA reports)
PULMONARY OEDEMA ( 16 FDA reports)
RECTAL HAEMORRHAGE ( 16 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 16 FDA reports)
ANGINA PECTORIS ( 15 FDA reports)
COGNITIVE DISORDER ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 15 FDA reports)
HAEMORRHOIDS ( 15 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 15 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 15 FDA reports)
LUNG NEOPLASM ( 15 FDA reports)
OEDEMA ( 15 FDA reports)
PALLOR ( 15 FDA reports)
POOR QUALITY SLEEP ( 15 FDA reports)
TROPONIN INCREASED ( 15 FDA reports)
ACUTE PSYCHOSIS ( 14 FDA reports)
AGRANULOCYTOSIS ( 14 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 14 FDA reports)
ANOREXIA ( 14 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 14 FDA reports)
CANDIDIASIS ( 14 FDA reports)
DECREASED INTEREST ( 14 FDA reports)
DROOLING ( 14 FDA reports)
FACIAL BONES FRACTURE ( 14 FDA reports)
HYPERTENSIVE CRISIS ( 14 FDA reports)
INCREASED APPETITE ( 14 FDA reports)
MUSCLE SPASMS ( 14 FDA reports)
MYOCARDIAL ISCHAEMIA ( 14 FDA reports)
OXYGEN SATURATION DECREASED ( 14 FDA reports)
POLYURIA ( 14 FDA reports)
PRURITUS ( 14 FDA reports)
TOOTH ABSCESS ( 14 FDA reports)
AFFECTIVE DISORDER ( 13 FDA reports)
APHASIA ( 13 FDA reports)
ARTHRALGIA ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
DRUG SCREEN POSITIVE ( 13 FDA reports)
GINGIVAL PAIN ( 13 FDA reports)
GYNAECOMASTIA ( 13 FDA reports)
HYPERPHAGIA ( 13 FDA reports)
HYPONATRAEMIA ( 13 FDA reports)
INCORRECT DOSE ADMINISTERED ( 13 FDA reports)
LEUKOCYTOSIS ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 13 FDA reports)
OFF LABEL USE ( 13 FDA reports)
OVERWEIGHT ( 13 FDA reports)
PLEUROTHOTONUS ( 13 FDA reports)
SLEEP APNOEA SYNDROME ( 13 FDA reports)
THIRST ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
ARTHROPATHY ( 12 FDA reports)
BLOOD BILIRUBIN INCREASED ( 12 FDA reports)
BONE PAIN ( 12 FDA reports)
BREAST CANCER RECURRENT ( 12 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 12 FDA reports)
CAESAREAN SECTION ( 12 FDA reports)
CARDIOMEGALY ( 12 FDA reports)
CONTUSION ( 12 FDA reports)
CRYING ( 12 FDA reports)
DIAPHRAGMATIC HERNIA ( 12 FDA reports)
DISABILITY ( 12 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 12 FDA reports)
EXPOSED BONE IN JAW ( 12 FDA reports)
GINGIVAL INFECTION ( 12 FDA reports)
HEPATITIS ( 12 FDA reports)
HOSTILITY ( 12 FDA reports)
HUMERUS FRACTURE ( 12 FDA reports)
HYPERCHOLESTEROLAEMIA ( 12 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 12 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
LOOSE TOOTH ( 12 FDA reports)
MENOPAUSAL SYMPTOMS ( 12 FDA reports)
METASTASES TO SPINE ( 12 FDA reports)
MULTIPLE DRUG OVERDOSE ( 12 FDA reports)
MYXOEDEMA COMA ( 12 FDA reports)
NASOPHARYNGITIS ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
OSTEONECROSIS OF JAW ( 12 FDA reports)
PEPTIC ULCER ( 12 FDA reports)
RASH PRURITIC ( 12 FDA reports)
SPINAL OSTEOARTHRITIS ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
TACHYPNOEA ( 12 FDA reports)
TENDONITIS ( 12 FDA reports)
ULCER ( 12 FDA reports)
WITHDRAWAL SYNDROME ( 12 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 11 FDA reports)
ANHEDONIA ( 11 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 11 FDA reports)
CHEST X-RAY ABNORMAL ( 11 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 11 FDA reports)
COMA ( 11 FDA reports)
COMMUNICATION DISORDER ( 11 FDA reports)
COMPULSIONS ( 11 FDA reports)
CREPITATIONS ( 11 FDA reports)
FAECAL INCONTINENCE ( 11 FDA reports)
HAEMATEMESIS ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
HISTOPLASMOSIS ( 11 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
OVARIAN CYST ( 11 FDA reports)
PELVIC PAIN ( 11 FDA reports)
PHARYNGITIS ( 11 FDA reports)
PLEURAL FIBROSIS ( 11 FDA reports)
RASH GENERALISED ( 11 FDA reports)
RENAL FAILURE CHRONIC ( 11 FDA reports)
SPLENIC LESION ( 11 FDA reports)
SPUTUM DISCOLOURED ( 11 FDA reports)
TOOTHACHE ( 11 FDA reports)
TYPE 1 DIABETES MELLITUS ( 11 FDA reports)
UTERINE HAEMORRHAGE ( 11 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 11 FDA reports)
VENTRICULAR HYPERTROPHY ( 11 FDA reports)
ALOPECIA ( 10 FDA reports)
BLOOD GLUCOSE DECREASED ( 10 FDA reports)
CHILLS ( 10 FDA reports)
COGWHEEL RIGIDITY ( 10 FDA reports)
DEPRESSIVE SYMPTOM ( 10 FDA reports)
FLUSHING ( 10 FDA reports)
HAEMODIALYSIS ( 10 FDA reports)
HEPATIC ENZYME INCREASED ( 10 FDA reports)
IDEAS OF REFERENCE ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
MITRAL VALVE INCOMPETENCE ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
MOVEMENT DISORDER ( 10 FDA reports)
MUSCLE TWITCHING ( 10 FDA reports)
MYASTHENIA GRAVIS ( 10 FDA reports)
PANCYTOPENIA ( 10 FDA reports)
PELVIC FRACTURE ( 10 FDA reports)
RASH MACULAR ( 10 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 10 FDA reports)
SELF-INJURIOUS IDEATION ( 10 FDA reports)
SUICIDAL BEHAVIOUR ( 10 FDA reports)
ABDOMINAL DISCOMFORT ( 9 FDA reports)
ALVEOLAR OSTEITIS ( 9 FDA reports)
AMMONIA INCREASED ( 9 FDA reports)
ATRIAL FIBRILLATION ( 9 FDA reports)
BRONCHOSPASM ( 9 FDA reports)
DIPLOPIA ( 9 FDA reports)
DISEASE RECURRENCE ( 9 FDA reports)
DRUG ABUSE ( 9 FDA reports)
DRUG ABUSER ( 9 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 9 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 9 FDA reports)
EPILEPSY ( 9 FDA reports)
ESSENTIAL HYPERTENSION ( 9 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 9 FDA reports)
HOT FLUSH ( 9 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 9 FDA reports)
INFLUENZA LIKE ILLNESS ( 9 FDA reports)
MAJOR DEPRESSION ( 9 FDA reports)
NECK PAIN ( 9 FDA reports)
OCCULT BLOOD POSITIVE ( 9 FDA reports)
PERIODONTITIS ( 9 FDA reports)
PITUITARY TUMOUR BENIGN ( 9 FDA reports)
SKIN LESION ( 9 FDA reports)
SPLENIC INJURY ( 9 FDA reports)
STARING ( 9 FDA reports)
AMENORRHOEA ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
BLOOD URINE PRESENT ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
CEREBRAL HAEMORRHAGE ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
CHOREA ( 8 FDA reports)
CHRONIC SINUSITIS ( 8 FDA reports)
CONDUCTION DISORDER ( 8 FDA reports)
DELUSION OF REFERENCE ( 8 FDA reports)
DERMATITIS ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DIABETIC RETINOPATHY ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 8 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 8 FDA reports)
EXOSTOSIS ( 8 FDA reports)
FLAT AFFECT ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 8 FDA reports)
GINGIVITIS ( 8 FDA reports)
GLYCOSURIA ( 8 FDA reports)
HALLUCINATION, OLFACTORY ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
HYDRONEPHROSIS ( 8 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 8 FDA reports)
HYPOKINESIA ( 8 FDA reports)
HYPOVOLAEMIA ( 8 FDA reports)
ILEUS PARALYTIC ( 8 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 8 FDA reports)
INDUCED LABOUR ( 8 FDA reports)
KIDNEY INFECTION ( 8 FDA reports)
LACERATION ( 8 FDA reports)
LOGORRHOEA ( 8 FDA reports)
LUMBAR RADICULOPATHY ( 8 FDA reports)
LYMPHADENITIS ( 8 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 8 FDA reports)
MASKED FACIES ( 8 FDA reports)
MYALGIA ( 8 FDA reports)
ORAL HERPES ( 8 FDA reports)
OTITIS MEDIA ACUTE ( 8 FDA reports)
POVERTY OF SPEECH ( 8 FDA reports)
PSORIASIS ( 8 FDA reports)
RHINITIS ALLERGIC ( 8 FDA reports)
SCHIZOAFFECTIVE DISORDER ( 8 FDA reports)
STATUS EPILEPTICUS ( 8 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 8 FDA reports)
TEARFULNESS ( 8 FDA reports)
THOUGHT BLOCKING ( 8 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 8 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 7 FDA reports)
BRUXISM ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CARDIAC FAILURE ACUTE ( 7 FDA reports)
COLITIS ISCHAEMIC ( 7 FDA reports)
DEAFNESS NEUROSENSORY ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DRUG INTOLERANCE ( 7 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 7 FDA reports)
DYSSTASIA ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
EYE DISORDER ( 7 FDA reports)
EYE IRRITATION ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HEART RATE IRREGULAR ( 7 FDA reports)
HEPATIC ENCEPHALOPATHY ( 7 FDA reports)
HEPATIC NECROSIS ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
INCOHERENT ( 7 FDA reports)
INITIAL INSOMNIA ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
LOCAL SWELLING ( 7 FDA reports)
LUNG NEOPLASM MALIGNANT ( 7 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MONOCYTE COUNT DECREASED ( 7 FDA reports)
MOOD SWINGS ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MYDRIASIS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
SERUM FERRITIN INCREASED ( 7 FDA reports)
SEXUALLY TRANSMITTED DISEASE ( 7 FDA reports)
SHOCK ( 7 FDA reports)
TORTICOLLIS ( 7 FDA reports)
TRANSAMINASES INCREASED ( 7 FDA reports)
UNEVALUABLE EVENT ( 7 FDA reports)
VITAMIN B12 INCREASED ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ABDOMINAL NEOPLASM ( 6 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DEMENTIA ( 6 FDA reports)
DIFFICULTY IN WALKING ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DRUG LEVEL DECREASED ( 6 FDA reports)
DYSLALIA ( 6 FDA reports)
DYSPHORIA ( 6 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
FLUID INTAKE REDUCED ( 6 FDA reports)
GASTRIC DISORDER ( 6 FDA reports)
GESTATIONAL DIABETES ( 6 FDA reports)
HALLUCINATIONS, MIXED ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
HYPOTHERMIA ( 6 FDA reports)
INAPPROPRIATE AFFECT ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
LIBIDO DECREASED ( 6 FDA reports)
LOWER LIMB FRACTURE ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MORBID THOUGHTS ( 6 FDA reports)
NEGATIVISM ( 6 FDA reports)
NEPHRITIS ( 6 FDA reports)
NEUTROPHILIA ( 6 FDA reports)
ORCHITIS ( 6 FDA reports)
PAROTID GLAND ENLARGEMENT ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PERICARDITIS ( 6 FDA reports)
PRESCRIBED OVERDOSE ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
PUPIL FIXED ( 6 FDA reports)
QRS AXIS ABNORMAL ( 6 FDA reports)
ROAD TRAFFIC ACCIDENT ( 6 FDA reports)
SALIVARY GLAND PAIN ( 6 FDA reports)
SCHIZOPHRENIA, RESIDUAL TYPE ( 6 FDA reports)
SCREAMING ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
TESTICULAR MASS ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 6 FDA reports)
UPPER LIMB FRACTURE ( 6 FDA reports)
VENOUS INSUFFICIENCY ( 6 FDA reports)
ABASIA ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 5 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
AKINESIA ( 5 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 5 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 5 FDA reports)
BLUNTED AFFECT ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
BREATH SOUNDS ABNORMAL ( 5 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 5 FDA reports)
CARDIOMYOPATHY ( 5 FDA reports)
CATARACT ( 5 FDA reports)
CHOREOATHETOSIS ( 5 FDA reports)
CONVERSION DISORDER ( 5 FDA reports)
DIABETIC NEUROPATHY ( 5 FDA reports)
DROP ATTACKS ( 5 FDA reports)
DRUG INTERACTION POTENTIATION ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ECHOLALIA ( 5 FDA reports)
EJECTION FRACTION ABNORMAL ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 5 FDA reports)
ENURESIS ( 5 FDA reports)
EPIDIDYMAL INFECTION ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEAD INJURY ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HERNIA ( 5 FDA reports)
HICCUPS ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERREFLEXIA ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
IMPAIRED HEALING ( 5 FDA reports)
INFLAMMATION ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LARYNGOSPASM ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 5 FDA reports)
MUTISM ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
NO THERAPEUTIC RESPONSE ( 5 FDA reports)
OBSESSIVE THOUGHTS ( 5 FDA reports)
OBSESSIVE-COMPULSIVE PERSONALITY DISORDER ( 5 FDA reports)
OPPOSITIONAL DEFIANT DISORDER ( 5 FDA reports)
PAIN IN JAW ( 5 FDA reports)
PATHOLOGICAL GAMBLING ( 5 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 5 FDA reports)
PRESSURE OF SPEECH ( 5 FDA reports)
PRIAPISM ( 5 FDA reports)
PROTRUSION TONGUE ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RESPIRATORY RATE INCREASED ( 5 FDA reports)
SALIVARY GLAND CALCULUS ( 5 FDA reports)
SEBACEOUS GLAND DISORDER ( 5 FDA reports)
SLEEP TALKING ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
THEFT ( 5 FDA reports)
THROMBOCYTHAEMIA ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
UTERINE CANCER ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
WATER INTOXICATION ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 4 FDA reports)
ADVERSE EVENT ( 4 FDA reports)
ANAPHYLACTOID REACTION ( 4 FDA reports)
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
APHTHOUS STOMATITIS ( 4 FDA reports)
APRAXIA ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
BENIGN COLONIC NEOPLASM ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BIOPSY LIVER ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BREAST TENDERNESS ( 4 FDA reports)
BRONCHITIS CHRONIC ( 4 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 4 FDA reports)
CARDIAC OPERATION ( 4 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 4 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 4 FDA reports)
DIABETIC ENCEPHALOPATHY ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DILATATION VENTRICULAR ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSTHYMIC DISORDER ( 4 FDA reports)
EAR PAIN ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
EJACULATION FAILURE ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
ERECTILE DYSFUNCTION ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXERCISE TOLERANCE DECREASED ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
EYE PRURITUS ( 4 FDA reports)
FAECALOMA ( 4 FDA reports)
FEELING HOT ( 4 FDA reports)
FEELINGS OF WORTHLESSNESS ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
GALLBLADDER DISORDER ( 4 FDA reports)
GASTROENTERITIS VIRAL ( 4 FDA reports)
GRANULOMA ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HAEMORRHAGIC STROKE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERKINETIC HEART SYNDROME ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERSOMNIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
IMPULSIVE BEHAVIOUR ( 4 FDA reports)
INCONTINENCE ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INSULIN RESISTANCE ( 4 FDA reports)
JOINT DISLOCATION ( 4 FDA reports)
JOINT STIFFNESS ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 4 FDA reports)
LABORATORY TEST INTERFERENCE ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
METASTASES TO LIVER ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 4 FDA reports)
MYOGLOBIN URINE PRESENT ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NERVOUS SYSTEM DISORDER ( 4 FDA reports)
OLIGOMENORRHOEA ( 4 FDA reports)
OTITIS EXTERNA ( 4 FDA reports)
PARKINSON'S DISEASE ( 4 FDA reports)
POISONING DELIBERATE ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PRURIGO ( 4 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 4 FDA reports)
PSYCHOSOMATIC DISEASE ( 4 FDA reports)
PSYCHOTIC BEHAVIOUR ( 4 FDA reports)
RECTAL CANCER STAGE IV ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SCAR ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 4 FDA reports)
SOMATIC DELUSION ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TOURETTE'S DISORDER ( 4 FDA reports)
TRISMUS ( 4 FDA reports)
TROPONIN I INCREASED ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 4 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ABORTION MISSED ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACETONAEMIA ( 3 FDA reports)
ACIDOSIS ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ADENOMA BENIGN ( 3 FDA reports)
ADJUSTMENT DISORDER ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ALCOHOLISM ( 3 FDA reports)
ANOGENITAL WARTS ( 3 FDA reports)
ANORGASMIA ( 3 FDA reports)
APHAGIA ( 3 FDA reports)
ARTERIAL HAEMORRHAGE ( 3 FDA reports)
ATELECTASIS ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 3 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BILE DUCT STONE ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE ORTHOSTATIC INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BRADYPHRENIA ( 3 FDA reports)
BREAST ENLARGEMENT ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BRUGADA SYNDROME ( 3 FDA reports)
BURNOUT SYNDROME ( 3 FDA reports)
CARDIAC DEATH ( 3 FDA reports)
CATAPLEXY ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CHOKING SENSATION ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLONUS ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CORNEAL DISORDER ( 3 FDA reports)
DELUSION OF GRANDEUR ( 3 FDA reports)
DEVELOPMENTAL DELAY ( 3 FDA reports)
DIET REFUSAL ( 3 FDA reports)
DILATATION ATRIAL ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
EPSTEIN-BARR VIRUS ANTIBODY POSITIVE ( 3 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 3 FDA reports)
EXCESSIVE EYE BLINKING ( 3 FDA reports)
FEEDING DISORDER NEONATAL ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
FOETAL MALFORMATION ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL INFECTION ( 3 FDA reports)
GINGIVITIS ULCERATIVE ( 3 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 3 FDA reports)
GLOSSODYNIA ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRANULOCYTE COUNT DECREASED ( 3 FDA reports)
HAEMOGLOBIN INCREASED ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HUNGER ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPERSEXUALITY ( 3 FDA reports)
HYPERTENSIVE HEART DISEASE ( 3 FDA reports)
HYPERTONIA ( 3 FDA reports)
HYPNAGOGIC HALLUCINATION ( 3 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOVENTILATION ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
KETOACIDOSIS ( 3 FDA reports)
LABILE BLOOD PRESSURE ( 3 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
LICE INFESTATION ( 3 FDA reports)
LIGAMENT SPRAIN ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIPIDS INCREASED ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MENSTRUATION IRREGULAR ( 3 FDA reports)
METASTASES TO PERITONEUM ( 3 FDA reports)
MIDDLE INSOMNIA ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 3 FDA reports)
MYOPIA ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ONYCHOMYCOSIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POSTURE ABNORMAL ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SCOTOMA ( 3 FDA reports)
SKIN PAPILLOMA ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SMALL FOR DATES BABY ( 3 FDA reports)
SPLENIC NECROSIS ( 3 FDA reports)
STEREOTYPY ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STUPOR ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TACITURNITY ( 3 FDA reports)
THERAPY REGIMEN CHANGED ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
URINARY HESITATION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR PRE-EXCITATION ( 3 FDA reports)
VISUAL ACUITY REDUCED ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME ( 3 FDA reports)
YAWNING ( 3 FDA reports)
ABNORMAL WEIGHT GAIN ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABULIA ( 2 FDA reports)
ACCOMMODATION DISORDER ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ALCOHOLIC SEIZURE ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPETITE DISORDER ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BELLIGERENCE ( 2 FDA reports)
BICUSPID AORTIC VALVE ( 2 FDA reports)
BILIARY TRACT DISORDER ( 2 FDA reports)
BLEPHARAL PAPILLOMA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD IRON DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BRAIN DEATH ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
CALCULUS URETHRAL ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL HYGROMA ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHEILOSIS ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLONOSCOPY ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DEPRESSION SUICIDAL ( 2 FDA reports)
DEREALISATION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DROWNING ( 2 FDA reports)
DRUG INTERACTION INHIBITION ( 2 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 2 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENDOMETRIAL DISORDER ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
EYE ALLERGY ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAMILY STRESS ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING OF DESPAIR ( 2 FDA reports)
FIBULA FRACTURE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HEAD BANGING ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HEAT STROKE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATITIS TOXIC ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
HODGKIN'S DISEASE ( 2 FDA reports)
HYPERINSULINAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
HYPOPLASTIC ANAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCISION SITE INFECTION ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 2 FDA reports)
JUDGEMENT IMPAIRED ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KYPHOSIS ( 2 FDA reports)
LIBIDO INCREASED ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOSS OF EMPLOYMENT ( 2 FDA reports)
LUPUS-LIKE SYNDROME ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
MACULOPATHY ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MASS ( 2 FDA reports)
MATERNAL USE OF ILLICIT DRUGS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUCOSAL EROSION ( 2 FDA reports)
MUMPS ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NAIL DISORDER ( 2 FDA reports)
NEONATAL DISORDER ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OBSTRUCTION GASTRIC ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 2 FDA reports)
PACHYGYRIA ( 2 FDA reports)
PANCREATITIS NECROTISING ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PAPILLOEDEMA ( 2 FDA reports)
PAPULE ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONIAN REST TREMOR ( 2 FDA reports)
PERIORBITAL OEDEMA ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHOBIA ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POLYHYDRAMNIOS ( 2 FDA reports)
PORIOMANIA ( 2 FDA reports)
PORTAL VEIN THROMBOSIS ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTICTAL STATE ( 2 FDA reports)
POTENTIATING DRUG INTERACTION ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PROTEIN C DECREASED ( 2 FDA reports)
PROTEIN S DECREASED ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PUPILS UNEQUAL ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
SARCOMA ( 2 FDA reports)
SCHIZOPHRENIA, DISORGANISED TYPE ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEPTUM PELLUCIDUM AGENESIS ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN HYPOPIGMENTATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SOCIAL PROBLEM ( 2 FDA reports)
SOMATIC HALLUCINATION ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL OSTEOMYELITIS ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SYDENHAM'S CHOREA ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TACHYPHRENIA ( 2 FDA reports)
TANGENTIALITY ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
TENSION HEADACHE ( 2 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 2 FDA reports)
THORACIC OPERATION ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TONGUE BITING ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRAUMATIC LUNG INJURY ( 2 FDA reports)
URETHRAL STENOSIS ( 2 FDA reports)
URINARY TRACT DISORDER ( 2 FDA reports)
UROBILINOGEN URINE ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WEIGHT BEARING DIFFICULTY ( 2 FDA reports)
WEIGHT FLUCTUATION ( 2 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL INJURY ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACANTHOSIS NIGRICANS ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
ADNEXA UTERI PAIN ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGITATION NEONATAL ( 1 FDA reports)
AGONAL RHYTHM ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ALCOHOL ABUSE ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ARTHRITIS REACTIVE ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT REPAIR ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTISM ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CORTISOL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE ( 1 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN DECREASED ( 1 FDA reports)
BLOOD THROMBOPLASTIN DECREASED ( 1 FDA reports)
BODY MASS INDEX INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYCARDIA NEONATAL ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
BURN OESOPHAGEAL ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CARDIAC MONITORING ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVIX CARCINOMA STAGE I ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COELIAC ARTERY OCCLUSION ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
COMPARTMENT SYNDROME ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPULSIVE LIP BITING ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONFABULATION ( 1 FDA reports)
CONGENITAL BLADDER ANOMALY ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONGENITAL EYE DISORDER ( 1 FDA reports)
CONGENITAL HEART VALVE DISORDER ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONVULSIVE THRESHOLD LOWERED ( 1 FDA reports)
CORNEAL EPITHELIUM DEFECT ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CREATINE URINE INCREASED ( 1 FDA reports)
CRIME ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYST ( 1 FDA reports)
CYSTOSARCOMA PHYLLODES ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED EYE CONTACT ( 1 FDA reports)
DECREASED VENTRICULAR PRELOAD ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATILLOMANIA ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETES WITH HYPEROSMOLARITY ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIAPHRAGMATIC INJURY ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSMORPHOPHOBIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPHEMIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ALLERGIC ( 1 FDA reports)
ENCOPRESIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHILIC MYOCARDITIS ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXCESSIVE SEXUAL FANTASIES ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INJURY ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALLOT'S TETRALOGY ( 1 FDA reports)
FEAR OF FALLING ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FINGER DEFORMITY ( 1 FDA reports)
FOETAL CHROMOSOME ABNORMALITY ( 1 FDA reports)
FOETAL DEATH ( 1 FDA reports)
FOETAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE DECREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL MALFORMATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLUCOSE URINE ( 1 FDA reports)
GRANDIOSITY ( 1 FDA reports)
GRIMACING ( 1 FDA reports)
GRIP STRENGTH DECREASED ( 1 FDA reports)
GROSS MOTOR DELAY ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEPATIC ARTERY OCCLUSION ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERINSULINISM ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INFANTILE APNOEIC ATTACK ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INSULINOMA ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KLEPTOMANIA ( 1 FDA reports)
KLINEFELTER'S SYNDROME ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACTATION DISORDER ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LEARNING DISABILITY ( 1 FDA reports)
LEARNING DISORDER ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOW BIRTH WEIGHT BABY ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MALFORMATION VENOUS ( 1 FDA reports)
MALLORY-WEISS SYNDROME ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTOID EFFUSION ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MONONUCLEOSIS HETEROPHILE TEST POSITIVE ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
NEGATIVE THOUGHTS ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NIGHT CRAMPS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NUCHAL RIGIDITY ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OBSESSIVE RUMINATION ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULOGYRIC CRISIS ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPTIC DISC DRUSEN ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 1 FDA reports)
OROMANDIBULAR DYSTONIA ( 1 FDA reports)
OROPHARYNGEAL BLISTERING ( 1 FDA reports)
ORTHOSTATIC HYPERTENSION ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDITIS CONSTRICTIVE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLAGIOCEPHALY ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POLYSUBSTANCE DEPENDENCE ( 1 FDA reports)
POOR PERSONAL HYGIENE ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRE-ECLAMPSIA ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSORIATIC ARTHROPATHY ( 1 FDA reports)
PSYCHOGENIC ERECTILE DYSFUNCTION ( 1 FDA reports)
PSYCHOSOCIAL SUPPORT ( 1 FDA reports)
PUBIS FRACTURE ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PURGING ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RABBIT SYNDROME ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL PIGMENTATION ( 1 FDA reports)
RETINITIS PIGMENTOSA ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCHIZOPHRENIA, CATATONIC TYPE ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEXUAL ACTIVITY INCREASED ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN ODOUR ABNORMAL ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY DECREASED ( 1 FDA reports)
SPINAL CORD INJURY CERVICAL ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUBMAXILLARY GLAND ENLARGEMENT ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN ONSET OF SLEEP ( 1 FDA reports)
SUPPORTIVE CARE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
TESTICULAR DISORDER ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THOUGHT BROADCASTING ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONGUE HAEMORRHAGE ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRAUMATIC LIVER INJURY ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
TRYPTASE INCREASED ( 1 FDA reports)
TUBEROUS SCLEROSIS ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY BLADDER RUPTURE ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL EXAMINATION ABNORMAL ( 1 FDA reports)
VASCULAR BYPASS GRAFT ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VICTIM OF ABUSE ( 1 FDA reports)
VISUAL ACUITY TESTS ABNORMAL ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VITAL CAPACITY ABNORMAL ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WOLFF-PARKINSON-WHITE SYNDROME CONGENITAL ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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