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

ABNORMAL BEHAVIOUR ( 228 FDA reports)
PYREXIA ( 85 FDA reports)
DELIRIUM ( 76 FDA reports)
HALLUCINATION ( 76 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 49 FDA reports)
CONVULSION ( 44 FDA reports)
PNEUMONIA ( 43 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 40 FDA reports)
AGITATION ( 32 FDA reports)
LOSS OF CONSCIOUSNESS ( 29 FDA reports)
DIZZINESS ( 26 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 25 FDA reports)
MALAISE ( 25 FDA reports)
CRYING ( 24 FDA reports)
ERYTHEMA MULTIFORME ( 23 FDA reports)
RESTLESSNESS ( 22 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
LIVER DISORDER ( 21 FDA reports)
VOMITING ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
BRONCHITIS ( 20 FDA reports)
SOMNOLENCE ( 20 FDA reports)
HEADACHE ( 19 FDA reports)
NAUSEA ( 19 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 19 FDA reports)
AGGRESSION ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
FEELING ABNORMAL ( 18 FDA reports)
RASH ( 17 FDA reports)
THROMBOCYTOPENIA ( 17 FDA reports)
CARDIO-RESPIRATORY ARREST ( 16 FDA reports)
SPEECH DISORDER ( 16 FDA reports)
TOXIC SKIN ERUPTION ( 16 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
FALL ( 15 FDA reports)
HYPOTHERMIA ( 15 FDA reports)
DYSPHONIA ( 14 FDA reports)
HALLUCINATION, VISUAL ( 14 FDA reports)
STEVENS-JOHNSON SYNDROME ( 14 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
EATING DISORDER ( 12 FDA reports)
HEPATITIS VIRAL ( 12 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 12 FDA reports)
INTERSTITIAL LUNG DISEASE ( 12 FDA reports)
MOUTH ULCERATION ( 12 FDA reports)
ORAL PAIN ( 12 FDA reports)
CYANOSIS ( 11 FDA reports)
DYSKINESIA ( 11 FDA reports)
NASOPHARYNGITIS ( 11 FDA reports)
PALLOR ( 11 FDA reports)
AMNESIA ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
SCREAMING ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
COUGH ( 9 FDA reports)
FEAR ( 9 FDA reports)
HALLUCINATION, AUDITORY ( 9 FDA reports)
LARYNGEAL OEDEMA ( 9 FDA reports)
MEMORY IMPAIRMENT ( 9 FDA reports)
STOMATITIS ( 9 FDA reports)
TREMOR ( 9 FDA reports)
URINARY RETENTION ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
CARDIAC ARREST ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
PSYCHIATRIC SYMPTOM ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
VISUAL DISTURBANCE ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
EPILEPSY ( 7 FDA reports)
EXCITABILITY ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
SHOCK ( 7 FDA reports)
SOMNAMBULISM ( 7 FDA reports)
TONGUE DISORDER ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG HYPERSENSITIVITY ( 6 FDA reports)
ECZEMA ( 6 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 6 FDA reports)
EPISTAXIS ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
HEPATITIS FULMINANT ( 6 FDA reports)
ILL-DEFINED DISORDER ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
LOGORRHOEA ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MENINGITIS FUNGAL ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESTLESS LEGS SYNDROME ( 6 FDA reports)
RHINORRHOEA ( 6 FDA reports)
TONGUE DISCOLOURATION ( 6 FDA reports)
ASTHMA ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
CHROMATURIA ( 5 FDA reports)
COGNITIVE DISORDER ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
FEBRILE CONVULSION ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
NO ADVERSE EVENT ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ADJUSTMENT DISORDER ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
CENTRAL OBESITY ( 4 FDA reports)
CUSHINGOID ( 4 FDA reports)
DELUSION ( 4 FDA reports)
DISSOCIATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
IMPLANT SITE EFFUSION ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
MIDDLE INSOMNIA ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PAIN ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SLEEP TERROR ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STRIDOR ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VASCULAR PURPURA ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ACIDOSIS ( 3 FDA reports)
ANTIBODY TEST POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 3 FDA reports)
DEATH ( 3 FDA reports)
DELIRIUM FEBRILE ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
INCOHERENT ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JOINT DISLOCATION ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MUMPS ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PERSECUTORY DELUSION ( 3 FDA reports)
PNEUMONIA MYCOPLASMAL ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
SKIN HYPERPIGMENTATION ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THROMBOSIS ( 3 FDA reports)
TORTICOLLIS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ASTEATOSIS ( 2 FDA reports)
ASTIGMATISM ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLAST CELLS PRESENT ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW TRANSPLANT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRONCHITIS ACUTE ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
COMPULSIONS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DREAMY STATE ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EAR DISORDER ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENANTHEMA ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FLAT AFFECT ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYDROCEPHALUS ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 2 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LARYNGOTRACHEO BRONCHITIS ( 2 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO ADRENALS ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NEUROSIS ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARASOMNIA ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PINEAL NEOPLASM ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PYELONEPHRITIS ( 2 FDA reports)
PYOMYOSITIS ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOLILOQUY ( 2 FDA reports)
STRABISMUS ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
THYROIDITIS ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VARICELLA ( 2 FDA reports)
VASCULAR OCCLUSION ( 2 FDA reports)
VENTRICULAR DRAINAGE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL CAVITY DRAINAGE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ABORTION THREATENED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ANALGESIC ASTHMA SYNDROME ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLEEDING TIME ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER REMOVAL ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CEREBROSPINAL FLUID RESERVOIR PLACEMENT ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL INCOMPETENCE ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COMA ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISUSE SYNDROME ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRODUODENAL ULCER ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPEREMESIS GRAVIDARUM ( 1 FDA reports)
HYPEREXPLEXIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPLANT SITE OEDEMA ( 1 FDA reports)
INAPPROPRIATE AFFECT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFANTILE SPASMS ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARYNGEAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL RETARDATION SEVERITY UNSPECIFIED ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOANING ( 1 FDA reports)
MUCOCUTANEOUS RASH ( 1 FDA reports)
MUCOSAL EXFOLIATION ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OVARIAN CANCER RECURRENT ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGEAL STENOSIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TONIC CONVULSION ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
TUMOUR NECROSIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 1 FDA reports)
VACCINATION COMPLICATION ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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