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

VOMITING ( 66 FDA reports)
PYREXIA ( 59 FDA reports)
ASTHENIA ( 54 FDA reports)
HEADACHE ( 51 FDA reports)
DIZZINESS ( 44 FDA reports)
DIARRHOEA ( 42 FDA reports)
DEATH ( 35 FDA reports)
SOMNOLENCE ( 30 FDA reports)
GAIT DISTURBANCE ( 29 FDA reports)
RHABDOMYOLYSIS ( 26 FDA reports)
ABDOMINAL PAIN ( 25 FDA reports)
GASTRITIS ( 25 FDA reports)
STRONGYLOIDIASIS ( 25 FDA reports)
ARTHRALGIA ( 24 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 24 FDA reports)
VISION BLURRED ( 24 FDA reports)
STEVENS-JOHNSON SYNDROME ( 23 FDA reports)
DEHYDRATION ( 22 FDA reports)
MUSCULAR WEAKNESS ( 21 FDA reports)
CONVULSION ( 20 FDA reports)
LOSS OF CONSCIOUSNESS ( 20 FDA reports)
MALAISE ( 20 FDA reports)
NAUSEA ( 19 FDA reports)
RASH ( 18 FDA reports)
SEPSIS ( 18 FDA reports)
URINARY INCONTINENCE ( 18 FDA reports)
GASTROENTERITIS ( 17 FDA reports)
DYSPNOEA ( 16 FDA reports)
MYALGIA ( 16 FDA reports)
FALL ( 15 FDA reports)
TREMOR ( 15 FDA reports)
SEDATION ( 14 FDA reports)
STILLBIRTH ( 14 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
INJECTION SITE PAIN ( 13 FDA reports)
OCULAR HYPERAEMIA ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
ABORTION SPONTANEOUS ( 12 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 12 FDA reports)
CONSTIPATION ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
DYSPHONIA ( 12 FDA reports)
EYE MOVEMENT DISORDER ( 12 FDA reports)
HELMINTHIC INFECTION ( 12 FDA reports)
INFLUENZA ( 12 FDA reports)
MENSTRUAL DISORDER ( 12 FDA reports)
MULTIPLE SCLEROSIS ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 11 FDA reports)
INJURY ( 11 FDA reports)
PAIN ( 11 FDA reports)
PALPITATIONS ( 11 FDA reports)
PRURITUS GENERALISED ( 11 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
COMA ( 10 FDA reports)
HYPOVOLAEMIC SHOCK ( 10 FDA reports)
JOINT SWELLING ( 10 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 10 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 10 FDA reports)
VISUAL ACUITY REDUCED ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
BACK PAIN ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DYSARTHRIA ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
MOUTH ULCERATION ( 9 FDA reports)
NEUTROPENIA ( 9 FDA reports)
ABDOMINAL DISTENSION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
EPILEPSY ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
MUCOSAL INFLAMMATION ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SKIN LESION ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
ADVERSE DRUG REACTION ( 7 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ASPHYXIA ( 7 FDA reports)
BRAIN OEDEMA ( 7 FDA reports)
CHOKING ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
GRAND MAL CONVULSION ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 7 FDA reports)
VISUAL IMPAIRMENT ( 7 FDA reports)
ACUTE RESPIRATORY FAILURE ( 6 FDA reports)
AGGRESSION ( 6 FDA reports)
APNOEA ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLISTER ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DERMATITIS BULLOUS ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSGEUSIA ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
MYOPATHY ( 6 FDA reports)
ODYNOPHAGIA ( 6 FDA reports)
PITTING OEDEMA ( 6 FDA reports)
PRODUCTIVE COUGH ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
RESTLESSNESS ( 6 FDA reports)
SEPTIC SHOCK ( 6 FDA reports)
SHOCK ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ABORTION INDUCED ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
BURNING SENSATION ( 5 FDA reports)
COUGH ( 5 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
FACIAL PAIN ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GLOSSITIS ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
OCULAR ICTERUS ( 5 FDA reports)
OESOPHAGITIS ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
RALES ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN ULCER ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BODY TINEA ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS EXFOLIATIVE ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENTEROBACTER BACTERAEMIA ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
EYE DISCHARGE ( 4 FDA reports)
EYE HAEMORRHAGE ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FUNGAL INFECTION ( 4 FDA reports)
GENERALISED ERYTHEMA ( 4 FDA reports)
GENITAL ULCERATION ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HICCUPS ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
IMMUNOSUPPRESSION ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MALARIA ( 4 FDA reports)
MAZZOTTI REACTION ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUROTOXICITY ( 4 FDA reports)
OLIGURIA ( 4 FDA reports)
ONYCHOMYCOSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PURPURA ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SCROTAL OEDEMA ( 4 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
SWELLING ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
ULCER ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
WEIGHT DECREASED ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
DELUSION ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
IRRITABLE BOWEL SYNDROME ( 3 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 3 FDA reports)
KLEBSIELLA BACTERAEMIA ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MICROSPORUM INFECTION ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYDRIASIS ( 3 FDA reports)
MYOPATHY TOXIC ( 3 FDA reports)
NEUROCYSTICERCOSIS ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
ORAL DISORDER ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
POLYHYDRAMNIOS ( 3 FDA reports)
PULMONARY MYCOSIS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
SKIN ATROPHY ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
UNRESPONSIVE TO STIMULI ( 3 FDA reports)
URINARY TRACT DISORDER ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
ABORTION SPONTANEOUS COMPLETE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CYST ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
ERUCTATION ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EYES SUNKEN ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GASTRIC ULCER PERFORATION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GUILLAIN-BARRE SYNDROME ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INJURY ASPHYXIATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POISONING ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULSE PRESSURE DECREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 2 FDA reports)
RHEUMATIC HEART DISEASE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE DRY ( 2 FDA reports)
YELLOW SKIN ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMMONIA INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASCARIASIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CONGENITAL HEARING DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA INFANTILE ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GAZE PALSY ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTION PROTOZOAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MICROSPORIDIA INFECTION ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PENILE PAIN ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PERSISTENT GENERALISED LYMPHADENOPATHY ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERINFECTION BACTERIAL ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THIRST ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXOPLASMOSIS ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URAEMIC ENCEPHALOPATHY ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL LOAD DECREASED ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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