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

DYSPNOEA ( 20 FDA reports)
FATIGUE ( 16 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
WEIGHT DECREASED ( 14 FDA reports)
ANAEMIA ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
COUGH ( 11 FDA reports)
PAIN ( 11 FDA reports)
CHEST PAIN ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
HEADACHE ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD UREA INCREASED ( 7 FDA reports)
BURNING SENSATION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
DRUG DEPENDENCE ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 6 FDA reports)
CARDIOMEGALY ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
HAEMATOCHEZIA ( 6 FDA reports)
HYPERHIDROSIS ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
INADEQUATE ANALGESIA ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DRUG TOXICITY ( 5 FDA reports)
FLUID OVERLOAD ( 5 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
RHINORRHOEA ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
WHEEZING ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CYSTIC FIBROSIS ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HILAR LYMPHADENOPATHY ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
LYMPHADENOPATHY ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
VITAL CAPACITY DECREASED ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE RESPIRATORY FAILURE ( 3 FDA reports)
ANGINA UNSTABLE ( 3 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CERVICOBRACHIAL SYNDROME ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIABETES MELLITUS ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG TOLERANCE ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
FALL ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HEPATOSPLENOMEGALY ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPERPHOSPHATAEMIA ( 3 FDA reports)
HYPERVENTILATION ( 3 FDA reports)
INCORRECT DOSE ADMINISTERED ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUMBAR RADICULOPATHY ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MOOD SWINGS ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PANIC ATTACK ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PERSONALITY CHANGE ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 3 FDA reports)
RADICULOPATHY ( 3 FDA reports)
RASH ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TENSION ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
TREMOR ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANOMALOUS PULMONARY VENOUS CONNECTION ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOVOLAEMIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MEGAKARYOCYTES INCREASED ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEUROPATHY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PARANOIA ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
REGURGITATION OF FOOD ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SNORING ( 2 FDA reports)
STEM CELL TRANSPLANT ( 2 FDA reports)
STRESS INCONTINENCE ( 2 FDA reports)
SUBCLAVIAN ARTERY THROMBOSIS ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIOVENOUS MALFORMATION ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD KETONE BODY ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BREAST NEOPLASM ( 1 FDA reports)
BRONCHIOLOALVEOLAR CARCINOMA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BUTTOCK PAIN ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIPHYSIOLYSIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HUNGER ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOSMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMPULSIVE BEHAVIOUR ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOEFFLER'S SYNDROME ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MAJOR DEPRESSION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MASS ( 1 FDA reports)
MEDIASTINAL DISORDER ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE MYELOMA ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NECK INJURY ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINALGIA ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONSILLAR DISORDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUNNEL VISION ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)