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

NEUTROPENIA ( 46 FDA reports)
PYREXIA ( 13 FDA reports)
VOMITING ( 13 FDA reports)
JAUNDICE ( 11 FDA reports)
ABORTION SPONTANEOUS ( 9 FDA reports)
DEATH ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
MALARIA ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
ANAEMIA ( 7 FDA reports)
HEADACHE ( 7 FDA reports)
CACHEXIA ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
BRONCHOPNEUMONIA ( 5 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
RASH PRURITIC ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
BACTERIAL SEPSIS ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
FRACTURE ( 4 FDA reports)
HEPATITIS ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ABORTION INCOMPLETE ( 3 FDA reports)
ASCITES ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RETINAL DETACHMENT ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TUBERCULOSIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BACTERIAL TOXAEMIA ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
STILLBIRTH ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TOXOPLASMOSIS ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSENTERY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FAILED INDUCTION OF LABOUR ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GENITAL LESION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PLASMODIUM FALCIPARUM INFECTION ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PREGNANCY INDUCED HYPERTENSION ( 1 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 1 FDA reports)
PREGNANCY WITH INJECTABLE CONTRACEPTIVE ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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